A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971640



Internal ID18606857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:33961405..33970053hg38UCSC Ensembl
Innerchr8:33818923..33827571hg19UCSC Ensembl
Innerchr8:33938465..33947113hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg388649
hg198649
hg188649
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2499895, nssv2499896, nssv2499893, nssv2499892, nssv2499891, nssv2499897, nssv2499899, nssv2499890, nssv2499894, nssv2499898
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)nsv971640
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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