A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983843



Internal ID18619035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73552567..73555640hg38UCSC Ensembl
Innerchr14:74019271..74022344hg19UCSC Ensembl
Innerchr14:73089024..73092097hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg383074
hg193074
hg183074
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1991297, nssv1991294, nssv1991292, nssv1991293, nssv1991296, nssv1991299, nssv1991300, nssv1991295, nssv1991301, nssv1991298
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHEATR4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983843
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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