A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526156



Internal ID15453449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:65940931..65973514hg38UCSC Ensembl
Innerchr2:66168065..66200648hg19UCSC Ensembl
Innerchr2:66021569..66054152hg18UCSC Ensembl
Innerchr2:66079716..66112299hg17UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3832584
hg1932584
hg1832584
hg1732584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702415
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526156
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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