A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976365



Internal ID18611571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:90762695..90774213hg38UCSC Ensembl
Innerchr14:91229039..91240557hg19UCSC Ensembl
Innerchr14:90298792..90310310hg18UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3811519
hg1911519
hg1811519
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1995221, nssv1995219, nssv1995227, nssv1995222, nssv1995224, nssv1995218, nssv1995223, nssv1995220, nssv1995226, nssv1995225
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesTTC7B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976365
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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