A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965215



Internal ID18600449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:139081423..139089772hg38UCSC Ensembl
Innerchr3:138800265..138808614hg19UCSC Ensembl
Innerchr3:140282955..140291304hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg388350
hg198350
hg188350
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2299786, nssv2299783, nssv2299779, nssv2299787, nssv2299788, nssv2299781, nssv2299782, nssv2299784, nssv2299780, nssv2299785
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)nsv965215
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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