A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965709



Internal ID18600939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32524612..32531080hg38UCSC Ensembl
Innerchr6:32492389..32498857hg19UCSC Ensembl
Innerchr6:32600367..32606835hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg386469
hg196469
hg186469
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2405780, nssv2405777, nssv2405781, nssv2405784, nssv2405779, nssv2405782, nssv2405776, nssv2405783, nssv2405775, nssv2405778
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHLA-DRB5
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965709
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer