A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981953



Internal ID18617149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:74504353..74510415hg38UCSC Ensembl
Innerchr8:75416588..75422650hg19UCSC Ensembl
Innerchr8:75579143..75585205hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg386063
hg196063
hg186063
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2507861, nssv2507856, nssv2507864, nssv2507862, nssv2507859, nssv2507860, nssv2507857, nssv2507863, nssv2507865, nssv2507858
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)nsv981953
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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