A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671804



Internal ID15061770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:203800763..203831298hg38UCSC Ensembl
Innerchr1:203769891..203800426hg19UCSC Ensembl
Innerchr1:202036514..202067049hg18UCSC Ensembl
Innerchr1:200501548..200532083hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3830536
hg1930536
hg1830536
hg1730536
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520482
Supporting Variants
Samples
Known GenesZC3H11A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671804
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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