A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967581



Internal ID18602809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40060337..40071347hg38UCSC Ensembl
Innerchr8:39917856..39928866hg19UCSC Ensembl
Innerchr8:40037013..40048023hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3811011
hg1911011
hg1811011
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2499855, nssv2499859, nssv2499851, nssv2499858, nssv2499856, nssv2499853, nssv2499854, nssv2499857, nssv2499852, nssv2499850
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)nsv967581
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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