A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974360



Internal ID18609571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:90107909..90108618hg38UCSC Ensembl
Innerchr14:90574253..90574962hg19UCSC Ensembl
Innerchr14:89644006..89644715hg18UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38710
hg19710
hg18710
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1995590, nssv1995587, nssv1995588, nssv1995594, nssv1995586, nssv1995595, nssv1995591, nssv1995593, nssv1995592, nssv1995589
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKCNK13
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974360
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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