A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967065



Internal ID18602294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:132242980..132244928hg38UCSC Ensembl
Innerchr3:131961824..131963772hg19UCSC Ensembl
Innerchr3:133444514..133446462hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381949
hg191949
hg181949
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2293859, nssv2293855, nssv2293856, nssv2293857, nssv2293860, nssv2293861, nssv2293853, nssv2293858, nssv2293854, nssv2293862
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)nsv967065
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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