A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981140



Internal ID18616339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:44088125..44092458hg38UCSC Ensembl
Innerchr6:44055862..44060195hg19UCSC Ensembl
Innerchr6:44163840..44168173hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg384334
hg194334
hg184334
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2407489, nssv2407488, nssv2407493, nssv2407496, nssv2407491, nssv2407497, nssv2407490, nssv2407494, nssv2407495, nssv2407492
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)nsv981140
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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