A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974354



Internal ID18609565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:81032535..81033949hg38UCSC Ensembl
Innerchr14:81498879..81500293hg19UCSC Ensembl
Innerchr14:80568632..80570046hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg381415
hg191415
hg181415
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1993113, nssv1993110, nssv1993119, nssv1993112, nssv1993114, nssv1993118, nssv1993111, nssv1993117, nssv1993115, nssv1993116
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesTSHR
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974354
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer