A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979839



Internal ID18615040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:63094049..63099212hg38UCSC Ensembl
Innerchr3:63079725..63084888hg19UCSC Ensembl
Innerchr3:63054765..63059928hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg385164
hg195164
hg185164
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2282769, nssv2282770, nssv2282774, nssv2282778, nssv2282775, nssv2282773, nssv2282776, nssv2282772, nssv2282777, nssv2282771
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)nsv979839
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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