A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974373



Internal ID18609584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102661647..102663914hg38UCSC Ensembl
Innerchr14:103127984..103130251hg19UCSC Ensembl
Innerchr14:102197737..102200004hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg382268
hg192268
hg182268
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1998425, nssv1998424, nssv1998422, nssv1998427, nssv1998421, nssv1998428, nssv1998420, nssv1998423, nssv1998419, nssv1998426
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRCOR1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974373
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