A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967066



Internal ID18602295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:134350718..134352416hg38UCSC Ensembl
Innerchr3:134069560..134071258hg19UCSC Ensembl
Innerchr3:135552250..135553948hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381699
hg191699
hg181699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2294065, nssv2294063, nssv2294059, nssv2294064, nssv2294067, nssv2294062, nssv2294066, nssv2294058, nssv2294061, nssv2294060
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)nsv967066
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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