A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698463



Internal ID15435115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:209151693..209169277hg38UCSC Ensembl
Innerchr1:209325038..209342622hg19UCSC Ensembl
Innerchr1:207391661..207409245hg18UCSC Ensembl
Innerchr1:205713433..205731017hg17UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3817585
hg1917585
hg1817585
hg1717585
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522816
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698463
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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