A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977493



Internal ID18612699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:86838155..86840227hg38UCSC Ensembl
Innerchr14:87304499..87306571hg19UCSC Ensembl
Innerchr14:86374252..86376324hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg382073
hg192073
hg182073
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1995661, nssv1995660, nssv1995658, nssv1995665, nssv1995657, nssv1995664, nssv1995659, nssv1995662, nssv1995666, nssv1995663
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)nsv977493
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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