A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967569



Internal ID18602797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:17149864..17150629hg38UCSC Ensembl
Innerchr8:17007373..17008138hg19UCSC Ensembl
Innerchr8:17051744..17052509hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38766
hg19766
hg18766
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2495349, nssv2495345, nssv2495351, nssv2495346, nssv2495344, nssv2495352, nssv2495348, nssv2495350, nssv2495347, nssv2495353
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)nsv967569
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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