A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518362



Internal ID15445655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:65760157..65841842hg38UCSC Ensembl
Innerchr2:65987291..66068976hg19UCSC Ensembl
Innerchr2:65840795..65922480hg18UCSC Ensembl
Innerchr2:65898942..65980627hg17UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3881686
hg1981686
hg1881686
hg1781686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695789
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518362
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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