A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966983



Internal ID18602212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18323..56449hg38UCSC Ensembl
Innerchr3:60001..98132hg19UCSC Ensembl
Innerchr3:35000..73132hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3838127
hg1938132
hg1838133
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2271795, nssv2271802, nssv2271799, nssv2271801, nssv2271796, nssv2271800, nssv2271794, nssv2271803, nssv2271797, nssv2271798
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)nsv966983
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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