A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967609



Internal ID18602837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:81627057..81628400hg38UCSC Ensembl
Innerchr8:82539292..82540635hg19UCSC Ensembl
Innerchr8:82701847..82703190hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg381344
hg191344
hg181344
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2510322, nssv2510327, nssv2510325, nssv2510320, nssv2510321, nssv2510318, nssv2510326, nssv2510323, nssv2510324, nssv2510319
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967609
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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