A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701571



Internal ID15091537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:161293590..161304521hg38UCSC Ensembl
Innerchr1:161263380..161274311hg19UCSC Ensembl
Innerchr1:159530004..159540935hg18UCSC Ensembl
Innerchr1:158076453..158087384hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3810932
hg1910932
hg1810932
hg1710932
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525443
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701571
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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