A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585272



Internal ID18883553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13193869..13850539hg38UCSC Ensembl
Innerchr21:14566190..15222860hg19UCSC Ensembl
Innerchr21:13488061..14144731hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38656671
hg19656671
hg18656671
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065793
Supporting Variants
Samples
Known GenesC21orf15, LOC100288966, MIR3156-3, MIR8069, POTED
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3585272
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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