A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519215



Internal ID15446508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:21250879..21279855hg38UCSC Ensembl
Innerchr2:21473751..21502727hg19UCSC Ensembl
Innerchr2:21327256..21356232hg18UCSC Ensembl
Innerchr2:21385403..21414379hg17UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3828977
hg1928977
hg1828977
hg1728977
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696704
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519215
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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