A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967620



Internal ID18602848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:99000902..99009106hg38UCSC Ensembl
Innerchr8:100013130..100021334hg19UCSC Ensembl
Innerchr8:100082306..100090510hg18UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg388205
hg198205
hg188205
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2514396, nssv2514395, nssv2514393, nssv2514397, nssv2514400, nssv2514402, nssv2514398, nssv2514399, nssv2514394, nssv2514401
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)nsv967620
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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