A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967073



Internal ID18255616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:139006440..139015560hg38UCSC Ensembl
Innerchr3:138725282..138734402hg19UCSC Ensembl
Innerchr3:140207972..140217092hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg389121
hg199121
hg189121
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2299676, nssv2299668, nssv2299670, nssv2299677, nssv2299674, nssv2299673, nssv2299669, nssv2299675, nssv2299671, nssv2299672
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)nsv967073
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer