A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967050



Internal ID18602279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:110682031..110683822hg38UCSC Ensembl
Innerchr3:110400878..110402669hg19UCSC Ensembl
Innerchr3:111883568..111885359hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg381792
hg191792
hg181792
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2288201, nssv2288200, nssv2288199, nssv2288202, nssv2288198, nssv2288193, nssv2288194, nssv2288196, nssv2288197, nssv2288195
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)nsv967050
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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