A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983845



Internal ID18619037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:81661912..81665059hg38UCSC Ensembl
Innerchr14:82128256..82131403hg19UCSC Ensembl
Innerchr14:81198009..81201156hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg383148
hg193148
hg183148
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1993511, nssv1993505, nssv1993507, nssv1993514, nssv1993506, nssv1993508, nssv1993513, nssv1993509, nssv1993510, nssv1993512
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)nsv983845
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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