A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583778



Internal ID18535373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10388379..10775598hg38UCSC Ensembl
Innerchr21:10736859..11124078hg19UCSC Ensembl
Innerchr21:9758730..10145949hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38387220
hg19387220
hg18387220
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059011
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)nssv3583778
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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