A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583746



Internal ID18882027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10458894..10775598hg38UCSC Ensembl
Innerchr21:10736859..11053563hg19UCSC Ensembl
Innerchr21:9758730..10075434hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38316705
hg19316705
hg18316705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062344
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)nssv3583746
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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