A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967032



Internal ID18602261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:81611855..81618364hg38UCSC Ensembl
Innerchr3:81661006..81667515hg19UCSC Ensembl
Innerchr3:81743696..81750205hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg386510
hg196510
hg186510
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2286448, nssv2286446, nssv2286442, nssv2286447, nssv2286449, nssv2286445, nssv2286443, nssv2286444, nssv2286441, nssv2286450
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGBE1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967032
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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