A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963355



Internal ID18598596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:120806122..120808952hg38UCSC Ensembl
Innerchr3:120524969..120527799hg19UCSC Ensembl
Innerchr3:122007659..122010489hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg382831
hg192831
hg182831
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2292670, nssv2292673, nssv2292674, nssv2292675, nssv2292668, nssv2292676, nssv2292672, nssv2292671, nssv2292667, nssv2292669
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)nsv963355
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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