A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976160



Internal ID18611367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18851206..18851934hg38UCSC Ensembl
Innerchr13:19425346..19426074hg19UCSC Ensembl
Innerchr13:18323346..18324074hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38729
hg19729
hg18729
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2619823, nssv2619827, nssv2619822, nssv2619821, nssv2619818, nssv2619826, nssv2619824, nssv2619819, nssv2619820, nssv2619825
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A9P
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976160
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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