A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967067



Internal ID18602296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:134383071..134385951hg38UCSC Ensembl
Innerchr3:134101913..134104793hg19UCSC Ensembl
Innerchr3:135584603..135587483hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg382881
hg192881
hg182881
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2294898, nssv2294894, nssv2294899, nssv2294892, nssv2294895, nssv2294891, nssv2294893, nssv2294900, nssv2294897, nssv2294896
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)nsv967067
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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