A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697308



Internal ID15433960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:11554211..11566801hg38UCSC Ensembl
Innerchr1:11614268..11626858hg19UCSC Ensembl
Innerchr1:11536855..11549445hg18UCSC Ensembl
Innerchr1:11548534..11561124hg17UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3812591
hg1912591
hg1812591
hg1712591
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520251
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697308
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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