A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526141



Internal ID15453434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:51869119..52035794hg38UCSC Ensembl
Innerchr2:52096257..52262932hg19UCSC Ensembl
Innerchr2:51949761..52116436hg18UCSC Ensembl
Innerchr2:52007908..52174583hg17UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38166676
hg19166676
hg18166676
hg17166676
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702396
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526141
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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