A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981106



Internal ID18616305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:17318353..17336912hg38UCSC Ensembl
Innerchr6:17318584..17337143hg19UCSC Ensembl
Innerchr6:17426563..17445122hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3818560
hg1918560
hg1818560
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2394421, nssv2394423, nssv2394426, nssv2394420, nssv2394425, nssv2394422, nssv2394429, nssv2394428, nssv2394427, nssv2394424
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)nsv981106
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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