A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977481



Internal ID18612687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:67615170..67617610hg38UCSC Ensembl
Innerchr14:68081887..68084327hg19UCSC Ensembl
Innerchr14:67151640..67154080hg18UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg382441
hg192441
hg182441
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1990681, nssv1990684, nssv1990689, nssv1990682, nssv1990680, nssv1990685, nssv1990688, nssv1990683, nssv1990686, nssv1990687
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)nsv977481
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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