U.S. flag

An official website of the United States government

nsv871976

  • Variant Calls:20
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:139,933

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1946 SVs from 94 studies. See in: genome view    
Remapped(Score: Perfect):103,586,151-103,726,083Question Mark
Overlapping variant regions from other studies: 1946 SVs from 94 studies. See in: genome view    
Remapped(Score: Perfect):104,128,773-104,268,705Question Mark
Overlapping variant regions from other studies: 1137 SVs from 28 studies. See in: genome view    
Submitted genomic103,930,296-104,070,228Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv871976RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nsv871976RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nsv871976Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1522628copy number lossSP53293SNP arraySNP genotyping analysis9
nssv1526353copy number lossSP57181SNP arraySNP genotyping analysis11
nssv1528039copy number lossSP81109SNP arraySNP genotyping analysis15
nssv1529734copy number gainMS10119SNP arraySNP genotyping analysis12
nssv1530124copy number lossMS10204SNP arraySNP genotyping analysis23
nssv1539766copy number lossMS14495SNP arraySNP genotyping analysis16
nssv1542154copy number gainMS15682SNP arraySNP genotyping analysis13
nssv1544526copy number gainMS16368SNP arraySNP genotyping analysis11
nssv1544852copy number gainMS16555SNP arraySNP genotyping analysis5
nssv1547523copy number gainMS17421SNP arraySNP genotyping analysis8
nssv1562945copy number lossMS25789SNP arraySNP genotyping analysis16
nssv1571207copy number lossIS32644SNP arraySNP genotyping analysis17
nssv1571808copy number lossIS32819SNP arraySNP genotyping analysis14
nssv1576392copy number gainIS34055SNP arraySNP genotyping analysis13
nssv1578266copy number gainIS34748SNP arraySNP genotyping analysis22
nssv1593079copy number lossIS39354SNP arraySNP genotyping analysis13
nssv1593210copy number gainIS39372SNP arraySNP genotyping analysis10
nssv1599304copy number lossIS41565SNP arraySNP genotyping analysis7
nssv1600627copy number gainIS41906SNP arraySNP genotyping analysis21
nssv1601019copy number lossIS41964SNP arraySNP genotyping analysis58

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1522628RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)del
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1526353RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)del
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1528039RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)del
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1529734RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)dup
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1530124RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)del
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1539766RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)del
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1542154RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)dup
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1544526RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)dup
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1544852RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)dup
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1547523RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)dup
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1562945RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)del
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1571207RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)del
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1571808RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)del
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1576392RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)dup
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1578266RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)dup
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1593079RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)del
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1593210RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)dup
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1599304RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)del
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1600627RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)dup
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1601019RemappedPerfectNC_000001.11:g.(10
3586151_103597390)
_(103719276_103726
083)del
GRCh38.p12First PassNC_000001.11Chr1103,586,151103,597,390103,719,276103,726,083
nssv1522628RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)del
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1526353RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)del
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1528039RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)del
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1529734RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)dup
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1530124RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)del
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1539766RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)del
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1542154RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)dup
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1544526RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)dup
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1544852RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)dup
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1547523RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)dup
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1562945RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)del
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1571207RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)del
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1571808RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)del
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1576392RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)dup
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1578266RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)dup
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1593079RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)del
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1593210RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)dup
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1599304RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)del
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1600627RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)dup
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1601019RemappedPerfectNC_000001.10:g.(10
4128773_104140012)
_(104261898_104268
705)del
GRCh37.p13First PassNC_000001.10Chr1104,128,773104,140,012104,261,898104,268,705
nssv1522628Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)del
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1526353Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)del
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1528039Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)del
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1529734Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)dup
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1530124Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)del
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1539766Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)del
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1542154Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)dup
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1544526Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)dup
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1544852Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)dup
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1547523Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)dup
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1562945Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)del
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1571207Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)del
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1571808Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)del
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1576392Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)dup
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1578266Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)dup
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1593079Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)del
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1593210Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)dup
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1599304Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)del
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1600627Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)dup
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228
nssv1601019Submitted genomicNC_000001.9:g.(103
930296_103941535)_
(104063421_1040702
28)del
NCBI36 (hg18)NC_000001.9Chr1103,930,296103,941,535104,063,421104,070,228

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

Support Center