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nsv888893

  • Variant Calls:13
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:39,041

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 423 SVs from 69 studies. See in: genome view    
Remapped(Score: Good):102,595,402-102,634,442Question Mark
Overlapping variant regions from other studies: 423 SVs from 69 studies. See in: genome view    
Remapped(Score: Good):102,235,849-102,274,889Question Mark
Overlapping variant regions from other studies: 218 SVs from 21 studies. See in: genome view    
Submitted genomic102,022,918-102,062,128Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv888893RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7102,595,402102,595,402102,634,442102,634,442
nsv888893RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7102,235,849102,235,849102,274,889102,274,889
nsv888893Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000007.12Chr7102,022,918102,032,517102,052,702102,062,128

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1504320copy number lossSP52431SNP arraySNP genotyping analysis12
nssv1509902copy number lossSP54956SNP arraySNP genotyping analysis783
nssv1544123copy number lossMS16266SNP arraySNP genotyping analysis9
nssv1546034copy number lossMS17113SNP arraySNP genotyping analysis12
nssv1552665copy number lossMS19582SNP arraySNP genotyping analysis12
nssv1558593copy number lossMS23412SNP arraySNP genotyping analysis11
nssv1567537copy number lossIS31113SNP arraySNP genotyping analysis7
nssv1574763copy number gainIS33622SNP arraySNP genotyping analysis12
nssv1579057copy number lossIS35010SNP arraySNP genotyping analysis9
nssv1582061copy number lossIS35783SNP arraySNP genotyping analysis8
nssv1591586copy number lossIS38994SNP arraySNP genotyping analysis6
nssv1598390copy number gainIS41166SNP arraySNP genotyping analysis14
nssv1600159copy number lossIS41852SNP arraySNP genotyping analysis6

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1504320RemappedGoodNC_000007.14:g.(10
2595402_102595402)
_(102634442_102634
442)del
GRCh38.p12First PassNC_000007.14Chr7102,595,402102,595,402102,634,442102,634,442
nssv1509902RemappedGoodNC_000007.14:g.(10
2595402_102595402)
_(102634442_102634
442)del
GRCh38.p12First PassNC_000007.14Chr7102,595,402102,595,402102,634,442102,634,442
nssv1544123RemappedGoodNC_000007.14:g.(10
2595402_102595402)
_(102634442_102634
442)del
GRCh38.p12First PassNC_000007.14Chr7102,595,402102,595,402102,634,442102,634,442
nssv1546034RemappedGoodNC_000007.14:g.(10
2595402_102595402)
_(102634442_102634
442)del
GRCh38.p12First PassNC_000007.14Chr7102,595,402102,595,402102,634,442102,634,442
nssv1552665RemappedGoodNC_000007.14:g.(10
2595402_102595402)
_(102634442_102634
442)del
GRCh38.p12First PassNC_000007.14Chr7102,595,402102,595,402102,634,442102,634,442
nssv1558593RemappedGoodNC_000007.14:g.(10
2595402_102595402)
_(102634442_102634
442)del
GRCh38.p12First PassNC_000007.14Chr7102,595,402102,595,402102,634,442102,634,442
nssv1567537RemappedGoodNC_000007.14:g.(10
2595402_102595402)
_(102634442_102634
442)del
GRCh38.p12First PassNC_000007.14Chr7102,595,402102,595,402102,634,442102,634,442
nssv1574763RemappedGoodNC_000007.14:g.(10
2595402_102595402)
_(102634442_102634
442)dup
GRCh38.p12First PassNC_000007.14Chr7102,595,402102,595,402102,634,442102,634,442
nssv1579057RemappedGoodNC_000007.14:g.(10
2595402_102595402)
_(102634442_102634
442)del
GRCh38.p12First PassNC_000007.14Chr7102,595,402102,595,402102,634,442102,634,442
nssv1582061RemappedGoodNC_000007.14:g.(10
2595402_102595402)
_(102634442_102634
442)del
GRCh38.p12First PassNC_000007.14Chr7102,595,402102,595,402102,634,442102,634,442
nssv1591586RemappedGoodNC_000007.14:g.(10
2595402_102595402)
_(102634442_102634
442)del
GRCh38.p12First PassNC_000007.14Chr7102,595,402102,595,402102,634,442102,634,442
nssv1598390RemappedGoodNC_000007.14:g.(10
2595402_102595402)
_(102634442_102634
442)dup
GRCh38.p12First PassNC_000007.14Chr7102,595,402102,595,402102,634,442102,634,442
nssv1600159RemappedGoodNC_000007.14:g.(10
2595402_102595402)
_(102634442_102634
442)del
GRCh38.p12First PassNC_000007.14Chr7102,595,402102,595,402102,634,442102,634,442
nssv1504320RemappedGoodNC_000007.13:g.(10
2235849_102235849)
_(102274889_102274
889)del
GRCh37.p13First PassNC_000007.13Chr7102,235,849102,235,849102,274,889102,274,889
nssv1509902RemappedGoodNC_000007.13:g.(10
2235849_102235849)
_(102274889_102274
889)del
GRCh37.p13First PassNC_000007.13Chr7102,235,849102,235,849102,274,889102,274,889
nssv1544123RemappedGoodNC_000007.13:g.(10
2235849_102235849)
_(102274889_102274
889)del
GRCh37.p13First PassNC_000007.13Chr7102,235,849102,235,849102,274,889102,274,889
nssv1546034RemappedGoodNC_000007.13:g.(10
2235849_102235849)
_(102274889_102274
889)del
GRCh37.p13First PassNC_000007.13Chr7102,235,849102,235,849102,274,889102,274,889
nssv1552665RemappedGoodNC_000007.13:g.(10
2235849_102235849)
_(102274889_102274
889)del
GRCh37.p13First PassNC_000007.13Chr7102,235,849102,235,849102,274,889102,274,889
nssv1558593RemappedGoodNC_000007.13:g.(10
2235849_102235849)
_(102274889_102274
889)del
GRCh37.p13First PassNC_000007.13Chr7102,235,849102,235,849102,274,889102,274,889
nssv1567537RemappedGoodNC_000007.13:g.(10
2235849_102235849)
_(102274889_102274
889)del
GRCh37.p13First PassNC_000007.13Chr7102,235,849102,235,849102,274,889102,274,889
nssv1574763RemappedGoodNC_000007.13:g.(10
2235849_102235849)
_(102274889_102274
889)dup
GRCh37.p13First PassNC_000007.13Chr7102,235,849102,235,849102,274,889102,274,889
nssv1579057RemappedGoodNC_000007.13:g.(10
2235849_102235849)
_(102274889_102274
889)del
GRCh37.p13First PassNC_000007.13Chr7102,235,849102,235,849102,274,889102,274,889
nssv1582061RemappedGoodNC_000007.13:g.(10
2235849_102235849)
_(102274889_102274
889)del
GRCh37.p13First PassNC_000007.13Chr7102,235,849102,235,849102,274,889102,274,889
nssv1591586RemappedGoodNC_000007.13:g.(10
2235849_102235849)
_(102274889_102274
889)del
GRCh37.p13First PassNC_000007.13Chr7102,235,849102,235,849102,274,889102,274,889
nssv1598390RemappedGoodNC_000007.13:g.(10
2235849_102235849)
_(102274889_102274
889)dup
GRCh37.p13First PassNC_000007.13Chr7102,235,849102,235,849102,274,889102,274,889
nssv1600159RemappedGoodNC_000007.13:g.(10
2235849_102235849)
_(102274889_102274
889)del
GRCh37.p13First PassNC_000007.13Chr7102,235,849102,235,849102,274,889102,274,889
nssv1504320Submitted genomicNC_000007.12:g.(10
2022918_102032517)
_(102052702_102062
128)del
NCBI36 (hg18)NC_000007.12Chr7102,022,918102,032,517102,052,702102,062,128
nssv1509902Submitted genomicNC_000007.12:g.(10
2022918_102032517)
_(102052702_102062
128)del
NCBI36 (hg18)NC_000007.12Chr7102,022,918102,032,517102,052,702102,062,128
nssv1544123Submitted genomicNC_000007.12:g.(10
2022918_102032517)
_(102052702_102062
128)del
NCBI36 (hg18)NC_000007.12Chr7102,022,918102,032,517102,052,702102,062,128
nssv1546034Submitted genomicNC_000007.12:g.(10
2022918_102032517)
_(102052702_102062
128)del
NCBI36 (hg18)NC_000007.12Chr7102,022,918102,032,517102,052,702102,062,128
nssv1552665Submitted genomicNC_000007.12:g.(10
2022918_102032517)
_(102052702_102062
128)del
NCBI36 (hg18)NC_000007.12Chr7102,022,918102,032,517102,052,702102,062,128
nssv1558593Submitted genomicNC_000007.12:g.(10
2022918_102032517)
_(102052702_102062
128)del
NCBI36 (hg18)NC_000007.12Chr7102,022,918102,032,517102,052,702102,062,128
nssv1567537Submitted genomicNC_000007.12:g.(10
2022918_102032517)
_(102052702_102062
128)del
NCBI36 (hg18)NC_000007.12Chr7102,022,918102,032,517102,052,702102,062,128
nssv1574763Submitted genomicNC_000007.12:g.(10
2022918_102032517)
_(102052702_102062
128)dup
NCBI36 (hg18)NC_000007.12Chr7102,022,918102,032,517102,052,702102,062,128
nssv1579057Submitted genomicNC_000007.12:g.(10
2022918_102032517)
_(102052702_102062
128)del
NCBI36 (hg18)NC_000007.12Chr7102,022,918102,032,517102,052,702102,062,128
nssv1582061Submitted genomicNC_000007.12:g.(10
2022918_102032517)
_(102052702_102062
128)del
NCBI36 (hg18)NC_000007.12Chr7102,022,918102,032,517102,052,702102,062,128
nssv1591586Submitted genomicNC_000007.12:g.(10
2022918_102032517)
_(102052702_102062
128)del
NCBI36 (hg18)NC_000007.12Chr7102,022,918102,032,517102,052,702102,062,128
nssv1598390Submitted genomicNC_000007.12:g.(10
2022918_102032517)
_(102052702_102062
128)dup
NCBI36 (hg18)NC_000007.12Chr7102,022,918102,032,517102,052,702102,062,128
nssv1600159Submitted genomicNC_000007.12:g.(10
2022918_102032517)
_(102052702_102062
128)del
NCBI36 (hg18)NC_000007.12Chr7102,022,918102,032,517102,052,702102,062,128

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

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