A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698024



Internal ID15434676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:61576174..61735826hg38UCSC Ensembl
Innerchr2:61803309..61962961hg19UCSC Ensembl
Innerchr2:61656813..61816465hg18UCSC Ensembl
Innerchr2:61714960..61874612hg17UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38159653
hg19159653
hg18159653
hg17159653
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521414
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698024
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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