A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521648



Internal ID15448941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:67639503..67640822hg38UCSC Ensembl
Innerchr1:68105186..68106505hg19UCSC Ensembl
Innerchr1:67877774..67879093hg18UCSC Ensembl
Innerchr1:67817207..67818526hg17UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381320
hg191320
hg181320
hg171320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698266
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521648
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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