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nsv900155

  • Variant Calls:20
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:86,375

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1349 SVs from 103 studies. See in: genome view    
Remapped(Score: Perfect):57,166,649-57,253,023Question Mark
Overlapping variant regions from other studies: 1349 SVs from 103 studies. See in: genome view    
Remapped(Score: Perfect):57,740,783-57,827,157Question Mark
Overlapping variant regions from other studies: 639 SVs from 35 studies. See in: genome view    
Submitted genomic56,638,784-56,725,158Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv900155RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nsv900155RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nsv900155Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1522128copy number lossSP52734SNP arraySNP genotyping analysis9
nssv1522427copy number lossSP53051SNP arraySNP genotyping analysis15
nssv1522459copy number lossSP53131SNP arraySNP genotyping analysis11
nssv1522882copy number lossSP53491SNP arraySNP genotyping analysis16
nssv1522904copy number lossSP53503SNP arraySNP genotyping analysis12
nssv1523193copy number lossSP53759SNP arraySNP genotyping analysis14
nssv1523629copy number lossSP54118SNP arraySNP genotyping analysis15
nssv1523698copy number lossSP54148SNP arraySNP genotyping analysis12
nssv1524515copy number lossSP55075SNP arraySNP genotyping analysis8
nssv1524843copy number lossSP55339SNP arraySNP genotyping analysis13
nssv1525634copy number lossSP56748SNP arraySNP genotyping analysis9
nssv1526236copy number lossSP57137SNP arraySNP genotyping analysis12
nssv1526767copy number lossSP57789SNP arraySNP genotyping analysis11
nssv1527067copy number lossSP58108SNP arraySNP genotyping analysis8
nssv1527524copy number lossSP58505SNP arraySNP genotyping analysis13
nssv1527739copy number lossSP80961SNP arraySNP genotyping analysis9
nssv1528413copy number lossSP81226SNP arraySNP genotyping analysis9
nssv1529060copy number lossSP81437SNP arraySNP genotyping analysis13
nssv1544938copy number lossMS16607SNP arraySNP genotyping analysis17
nssv1561886copy number lossMS25280SNP arraySNP genotyping analysis10

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1522128RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1522427RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1522459RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1522882RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1522904RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1523193RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1523629RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1523698RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1524515RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1524843RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1525634RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1526236RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1526767RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1527067RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1527524RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1527739RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1528413RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1529060RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1544938RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1561886RemappedPerfectNC_000013.11:g.(57
166649_57174660)_(
57250022_57253023)
del
GRCh38.p12First PassNC_000013.11Chr1357,166,64957,174,66057,250,02257,253,023
nssv1522128RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1522427RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1522459RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1522882RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1522904RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1523193RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1523629RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1523698RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1524515RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1524843RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1525634RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1526236RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1526767RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1527067RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1527524RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1527739RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1528413RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1529060RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1544938RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1561886RemappedPerfectNC_000013.10:g.(57
740783_57748794)_(
57824156_57827157)
del
GRCh37.p13First PassNC_000013.10Chr1357,740,78357,748,79457,824,15657,827,157
nssv1522128Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1522427Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1522459Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1522882Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1522904Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1523193Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1523629Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1523698Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1524515Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1524843Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1525634Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1526236Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1526767Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1527067Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1527524Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1527739Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1528413Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1529060Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1544938Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158
nssv1561886Submitted genomicNC_000013.9:g.(566
38784_56646795)_(5
6722157_56725158)d
el
NCBI36 (hg18)NC_000013.9Chr1356,638,78456,646,79556,722,15756,725,158

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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