A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963298



Internal ID18598539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13224527..13228569hg38UCSC Ensembl
Innerchr3:13266027..13270069hg19UCSC Ensembl
Innerchr3:13241027..13245069hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg384043
hg194043
hg184043
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2274031, nssv2274034, nssv2274032, nssv2274030, nssv2274037, nssv2274035, nssv2274028, nssv2274036, nssv2274033, nssv2274029
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)nsv963298
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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