A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692771



Internal ID15429423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130186696..130836347hg38UCSC Ensembl
Innerchr10:131984960..132634610hg19UCSC Ensembl
Innerchr10:131874950..132524600hg18UCSC Ensembl
Innerchr10:131874950..132524600hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38649652
hg19649651
hg18649651
hg17649651
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516699
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692771
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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