A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697839



Internal ID15434491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:11060221..11065233hg38UCSC Ensembl
Innerchr2:11200347..11205359hg19UCSC Ensembl
Innerchr2:11117798..11122810hg18UCSC Ensembl
Innerchr2:11150945..11155957hg17UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg385013
hg195013
hg185013
hg175013
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516163
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697839
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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