A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520657



Internal ID15447950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:16005395..16009658hg38UCSC Ensembl
Innerchr2:16145517..16149780hg19UCSC Ensembl
Innerchr2:16062968..16067231hg18UCSC Ensembl
Innerchr2:16096115..16100378hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg384264
hg194264
hg184264
hg174264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673619, nssv675260
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520657
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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