A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062344



Internal ID19151563
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 StatusM
Merged Variantsdgv4353n100
Supporting Variantsnssv3583746
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)nsv1062344
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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