A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967608



Internal ID18602836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:81521062..81522103hg38UCSC Ensembl
Innerchr8:82433297..82434338hg19UCSC Ensembl
Innerchr8:82595852..82596893hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg381042
hg191042
hg181042
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2510222, nssv2510230, nssv2510224, nssv2510223, nssv2510229, nssv2510226, nssv2510228, nssv2510225, nssv2510221, nssv2510227
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)nsv967608
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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