A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701259



Internal ID15091225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43403599..43409207hg38UCSC Ensembl
Innerchr21:44823479..44829087hg19UCSC Ensembl
Innerchr21:43647907..43653515hg18UCSC Ensembl
Innerchr21:43647907..43653515hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg385609
hg195609
hg185609
hg175609
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516339
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701259
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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