A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697612



Internal ID15434264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:27532525..27549971hg38UCSC Ensembl
Innerchr1:27859036..27876482hg19UCSC Ensembl
Innerchr1:27731623..27749069hg18UCSC Ensembl
Innerchr1:27543178..27560624hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3817447
hg1917447
hg1817447
hg1717447
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520790
Supporting Variants
Samples
Known GenesAHDC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697612
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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