A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519580



Internal ID15100187
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705456, nssv656960, nssv676630, nssv662919, nssv662308, nssv698683, nssv677440
Samples
Known GenesWDR78
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519580
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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