A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697899



Internal ID15087865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:32780171..32883398hg38UCSC Ensembl
Innerchr2:33005238..33108465hg19UCSC Ensembl
Innerchr2:32858742..32961969hg18UCSC Ensembl
Innerchr2:32916889..33020116hg17UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38103228
hg19103228
hg18103228
hg17103228
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516173
Supporting Variants
Samples
Known GenesLINC00486, TTC27
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697899
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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