A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970107



Internal ID18605331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32758830..32759503hg38UCSC Ensembl
Innerchr6:32726607..32727280hg19UCSC Ensembl
Innerchr6:32834585..32835258hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38674
hg19674
hg18674
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2404671, nssv2404669, nssv2404670, nssv2404672, nssv2404668, nssv2404667, nssv2404666, nssv2404673, nssv2404665, nssv2404664
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHLA-DQB2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970107
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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