A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979817



Internal ID18268332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32635237..32639861hg38UCSC Ensembl
Innerchr3:32676729..32681353hg19UCSC Ensembl
Innerchr3:32651733..32656357hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg384625
hg194625
hg184625
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2277800, nssv2277805, nssv2277804, nssv2277802, nssv2277807, nssv2277801, nssv2277803, nssv2277806, nssv2277809, nssv2277808
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)nsv979817
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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