A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977454



Internal ID18612660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34920690..34921555hg38UCSC Ensembl
Innerchr14:35389896..35390761hg19UCSC Ensembl
Innerchr14:34459647..34460512hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38866
hg19866
hg18866
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1983353, nssv1983351, nssv1983350, nssv1983349, nssv1983354, nssv1983358, nssv1983356, nssv1983355, nssv1983352, nssv1983357
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)nsv977454
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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