A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583779



Internal ID18882060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10386269..10775598hg38UCSC Ensembl
Innerchr21:10736859..11126188hg19UCSC Ensembl
Innerchr21:9758730..10148059hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38389330
hg19389330
hg18389330
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060652
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)nssv3583779
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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