A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965703



Internal ID18254247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29874997..29896765hg38UCSC Ensembl
Innerchr6:29842774..29864542hg19UCSC Ensembl
Innerchr6:29950753..29972521hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3821769
hg1921769
hg1821769
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2403124, nssv2403120, nssv2403122, nssv2403119, nssv2403116, nssv2403117, nssv2403123, nssv2403115, nssv2403121, nssv2403118
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHLA-H
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965703
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