A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660995



Internal ID15397647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13571018..13733164hg38UCSC Ensembl
Innerchr21:14943339..15105485hg19UCSC Ensembl
Innerchr21:13865210..14027356hg18UCSC Ensembl
Innerchr21:13865210..14027356hg17UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38162147
hg19162147
hg18162147
hg17162147
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515654
Supporting Variants
Samples
Known GenesLOC100288966, MIR8069, POTED
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660995
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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