A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705938



Internal ID15442590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:223874196..223887781hg38UCSC Ensembl
Innerchr1:224061898..224075483hg19UCSC Ensembl
Innerchr1:222128521..222142106hg18UCSC Ensembl
Innerchr1:220368633..220382218hg17UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3813586
hg1913586
hg1813586
hg1713586
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522556
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705938
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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