A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059011



Internal ID18801542
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 StatusM
Merged Variantsdgv4355n100
Supporting Variantsnssv3583778
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)nsv1059011
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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