A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585113



Internal ID18536708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10420787..10524078hg38UCSC Ensembl
Innerchr21:10988379..11091670hg19UCSC Ensembl
Innerchr21:10010250..10113541hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38103292
hg19103292
hg18103292
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060181
Supporting Variants
Samples
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5, TPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3585113
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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