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nsv882731

  • Variant Calls:6
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,579

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 213 SVs from 48 studies. See in: genome view    
Remapped(Score: Perfect):115,366,806-115,385,384Question Mark
Overlapping variant regions from other studies: 213 SVs from 48 studies. See in: genome view    
Remapped(Score: Perfect):114,702,503-114,721,081Question Mark
Overlapping variant regions from other studies: 65 SVs from 15 studies. See in: genome view    
Submitted genomic114,730,402-114,748,980Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv882731RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr5115,366,806115,371,714115,383,894115,385,384
nsv882731RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5114,702,503114,707,411114,719,591114,721,081
nsv882731Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000005.8Chr5114,730,402114,735,310114,747,490114,748,980

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1500829copy number lossSP50921SNP arraySNP genotyping analysis20
nssv1503254copy number lossSP52019SNP arraySNP genotyping analysis22
nssv1505293copy number lossSP53349SNP arraySNP genotyping analysis19
nssv1505703copy number lossSP53863SNP arraySNP genotyping analysis14
nssv1518134copy number lossSP57469SNP arraySNP genotyping analysis98
nssv1519103copy number lossSP80955SNP arraySNP genotyping analysis17

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1500829RemappedPerfectNC_000005.10:g.(11
5366806_115371714)
_(115383894_115385
384)del
GRCh38.p12First PassNC_000005.10Chr5115,366,806115,371,714115,383,894115,385,384
nssv1503254RemappedPerfectNC_000005.10:g.(11
5366806_115371714)
_(115383894_115385
384)del
GRCh38.p12First PassNC_000005.10Chr5115,366,806115,371,714115,383,894115,385,384
nssv1505293RemappedPerfectNC_000005.10:g.(11
5366806_115371714)
_(115383894_115385
384)del
GRCh38.p12First PassNC_000005.10Chr5115,366,806115,371,714115,383,894115,385,384
nssv1505703RemappedPerfectNC_000005.10:g.(11
5366806_115371714)
_(115383894_115385
384)del
GRCh38.p12First PassNC_000005.10Chr5115,366,806115,371,714115,383,894115,385,384
nssv1518134RemappedPerfectNC_000005.10:g.(11
5366806_115371714)
_(115383894_115385
384)del
GRCh38.p12First PassNC_000005.10Chr5115,366,806115,371,714115,383,894115,385,384
nssv1519103RemappedPerfectNC_000005.10:g.(11
5366806_115371714)
_(115383894_115385
384)del
GRCh38.p12First PassNC_000005.10Chr5115,366,806115,371,714115,383,894115,385,384
nssv1500829RemappedPerfectNC_000005.9:g.(114
702503_114707411)_
(114719591_1147210
81)del
GRCh37.p13First PassNC_000005.9Chr5114,702,503114,707,411114,719,591114,721,081
nssv1503254RemappedPerfectNC_000005.9:g.(114
702503_114707411)_
(114719591_1147210
81)del
GRCh37.p13First PassNC_000005.9Chr5114,702,503114,707,411114,719,591114,721,081
nssv1505293RemappedPerfectNC_000005.9:g.(114
702503_114707411)_
(114719591_1147210
81)del
GRCh37.p13First PassNC_000005.9Chr5114,702,503114,707,411114,719,591114,721,081
nssv1505703RemappedPerfectNC_000005.9:g.(114
702503_114707411)_
(114719591_1147210
81)del
GRCh37.p13First PassNC_000005.9Chr5114,702,503114,707,411114,719,591114,721,081
nssv1518134RemappedPerfectNC_000005.9:g.(114
702503_114707411)_
(114719591_1147210
81)del
GRCh37.p13First PassNC_000005.9Chr5114,702,503114,707,411114,719,591114,721,081
nssv1519103RemappedPerfectNC_000005.9:g.(114
702503_114707411)_
(114719591_1147210
81)del
GRCh37.p13First PassNC_000005.9Chr5114,702,503114,707,411114,719,591114,721,081
nssv1500829Submitted genomicNC_000005.8:g.(114
730402_114735310)_
(114747490_1147489
80)del
NCBI36 (hg18)NC_000005.8Chr5114,730,402114,735,310114,747,490114,748,980
nssv1503254Submitted genomicNC_000005.8:g.(114
730402_114735310)_
(114747490_1147489
80)del
NCBI36 (hg18)NC_000005.8Chr5114,730,402114,735,310114,747,490114,748,980
nssv1505293Submitted genomicNC_000005.8:g.(114
730402_114735310)_
(114747490_1147489
80)del
NCBI36 (hg18)NC_000005.8Chr5114,730,402114,735,310114,747,490114,748,980
nssv1505703Submitted genomicNC_000005.8:g.(114
730402_114735310)_
(114747490_1147489
80)del
NCBI36 (hg18)NC_000005.8Chr5114,730,402114,735,310114,747,490114,748,980
nssv1518134Submitted genomicNC_000005.8:g.(114
730402_114735310)_
(114747490_1147489
80)del
NCBI36 (hg18)NC_000005.8Chr5114,730,402114,735,310114,747,490114,748,980
nssv1519103Submitted genomicNC_000005.8:g.(114
730402_114735310)_
(114747490_1147489
80)del
NCBI36 (hg18)NC_000005.8Chr5114,730,402114,735,310114,747,490114,748,980

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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