A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970083



Internal ID18605307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26158062..26158924hg38UCSC Ensembl
Innerchr6:26158290..26159152hg19UCSC Ensembl
Innerchr6:26266269..26267131hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38863
hg19863
hg18863
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2396263, nssv2396270, nssv2396262, nssv2396271, nssv2396265, nssv2396268, nssv2396269, nssv2396264, nssv2396267, nssv2396266
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHIST1H2BD
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970083
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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