A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683210



Internal ID15073176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:14242899..14287033hg38UCSC Ensembl
Innerchr21:15615220..15659354hg19UCSC Ensembl
Innerchr21:14537091..14581225hg18UCSC Ensembl
Innerchr21:14537091..14581225hg17UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3844135
hg1944135
hg1844135
hg1744135
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520538
Supporting Variants
Samples
Known GenesABCC13
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683210
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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