A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967615



Internal ID18602843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:89412607..89417145hg38UCSC Ensembl
Innerchr8:90424836..90429374hg19UCSC Ensembl
Innerchr8:90493952..90498490hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg384539
hg194539
hg184539
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2513144, nssv2513137, nssv2513135, nssv2513140, nssv2513139, nssv2513143, nssv2513136, nssv2513141, nssv2513142, nssv2513138
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)nsv967615
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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