A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982292



Internal ID18617487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64348610..64501791hg38UCSC Ensembl
Innerchr9:69361028..69514209hg19UCSC Ensembl
Innerchr9:68650848..68804029hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38153182
hg19153182
hg18153182
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2549466, nssv2549464, nssv2549470, nssv2549463, nssv2549467, nssv2549461, nssv2549469, nssv2549462, nssv2549465, nssv2549468
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982292
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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