A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974363



Internal ID18262888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:90271786..90272659hg38UCSC Ensembl
Innerchr14:90738130..90739003hg19UCSC Ensembl
Innerchr14:89807883..89808756hg18UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38874
hg19874
hg18874
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1994706, nssv1994709, nssv1994712, nssv1994707, nssv1994714, nssv1994710, nssv1994708, nssv1994711, nssv1994713, nssv1994715
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPSMC1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974363
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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