A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662919



Internal ID15052885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:66816506..66828460hg38UCSC Ensembl
Innerchr1:67282189..67294143hg19UCSC Ensembl
Innerchr1:67054777..67066731hg18UCSC Ensembl
Innerchr1:66994210..67006164hg17UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3811955
hg1911955
hg1811955
hg1711955
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519580
Supporting Variants
Samples
Known GenesWDR78
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662919
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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