A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585152



Internal ID18536747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10338676..10510446hg38UCSC Ensembl
Innerchr21:11002011..11173781hg19UCSC Ensembl
Innerchr21:10023882..10195652hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38171771
hg19171771
hg18171771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063631
Supporting Variants
Samples
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3585152
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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