A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965213



Internal ID18600447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:136201394..136207078hg38UCSC Ensembl
Innerchr3:135920236..135925920hg19UCSC Ensembl
Innerchr3:137402926..137408610hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg385685
hg195685
hg185685
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2295929, nssv2295923, nssv2295924, nssv2295928, nssv2295931, nssv2295930, nssv2295932, nssv2295925, nssv2295926, nssv2295927
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)nsv965213
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