A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656960



Internal ID15046926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:66816506..66828380hg38UCSC Ensembl
Innerchr1:67282189..67294063hg19UCSC Ensembl
Innerchr1:67054777..67066651hg18UCSC Ensembl
Innerchr1:66994210..67006084hg17UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3811875
hg1911875
hg1811875
hg1711875
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)nssv656960
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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