A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583741



Internal ID18882022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10469623..10775598hg38UCSC Ensembl
Innerchr21:10736859..11042834hg19UCSC Ensembl
Innerchr21:9758730..10064705hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38305976
hg19305976
hg18305976
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057189
Supporting Variants
Samples
Known GenesBAGE2, 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)nssv3583741
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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