A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519160



Internal ID15446453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:11065233..11068168hg38UCSC Ensembl
Innerchr2:11205359..11208294hg19UCSC Ensembl
Innerchr2:11122810..11125745hg18UCSC Ensembl
Innerchr2:11155957..11158892hg17UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg382936
hg192936
hg182936
hg172936
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv211n21
Supporting Variantsnssv696640
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519160
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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