A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524209



Internal ID15451502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:236885902..236899679hg38UCSC Ensembl
Innerchr2:237794545..237808322hg19UCSC Ensembl
Innerchr2:237459284..237473061hg18UCSC Ensembl
Innerchr2:237576545..237590322hg17UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3813778
hg1913778
hg1813778
hg1713778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700096
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524209
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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