A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971636



Internal ID18606853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:33011028..33027357hg38UCSC Ensembl
Innerchr8:32868546..32884875hg19UCSC Ensembl
Innerchr8:32988088..33004417hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3816330
hg1916330
hg1816330
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2499301, nssv2499304, nssv2499307, nssv2499299, nssv2499300, nssv2499305, nssv2499303, nssv2499302, nssv2499298, nssv2499306
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)nsv971636
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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