A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519097



Internal ID15446390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:155963073..155986312hg38UCSC Ensembl
Innerchr2:156819585..156842824hg19UCSC Ensembl
Innerchr2:156527831..156551070hg18UCSC Ensembl
Innerchr2:156645093..156668332hg17UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3823240
hg1923240
hg1823240
hg1723240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696571
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519097
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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