A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974326



Internal ID18609537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:36010304..36012406hg38UCSC Ensembl
Innerchr14:36479510..36481612hg19UCSC Ensembl
Innerchr14:35549261..35551363hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg382103
hg192103
hg182103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1983643, nssv1983640, nssv1983641, nssv1983638, nssv1983642, nssv1983646, nssv1983639, nssv1983645, nssv1983644, nssv1983647
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)nsv974326
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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