A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970102



Internal ID18605326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29744998..29745802hg38UCSC Ensembl
Innerchr6:29712775..29713579hg19UCSC Ensembl
Innerchr6:29820754..29821558hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38805
hg19805
hg18805
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2401504, nssv2401503, nssv2401505, nssv2401498, nssv2401496, nssv2401499, nssv2401497, nssv2401502, nssv2401500, nssv2401501
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHLA-F-AS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970102
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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