A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967002



Internal ID18602231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35212382..35220794hg38UCSC Ensembl
Innerchr3:35253874..35262286hg19UCSC Ensembl
Innerchr3:35228878..35237290hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg388413
hg198413
hg188413
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2277644, nssv2277640, nssv2277639, nssv2277638, nssv2277641, nssv2277642, nssv2277637, nssv2277643, nssv2277636, nssv2277635
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)nsv967002
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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