A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965226



Internal ID18600460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:157161059..157163967hg38UCSC Ensembl
Innerchr3:156878848..156881756hg19UCSC Ensembl
Innerchr3:158361542..158364450hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg382909
hg192909
hg182909
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2302636, nssv2302641, nssv2302643, nssv2302644, nssv2302645, nssv2302640, nssv2302639, nssv2302637, nssv2302638, nssv2302642
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)nsv965226
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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