A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521067



Internal ID15448360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:8837640..8838546hg38UCSC Ensembl
Innerchr2:8977770..8978676hg19UCSC Ensembl
Innerchr2:8895221..8896127hg18UCSC Ensembl
Innerchr2:8928368..8929274hg17UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38907
hg19907
hg18907
hg17907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697766
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521067
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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