A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963309



Internal ID18251864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:39333124..39373689hg38UCSC Ensembl
Innerchr3:39374615..39415180hg19UCSC Ensembl
Innerchr3:39349619..39390184hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3840566
hg1940566
hg1840566
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2279300, nssv2279298, nssv2279303, nssv2279302, nssv2279306, nssv2279304, nssv2279305, nssv2279299, nssv2279301, nssv2279297
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCCR8
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963309
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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