A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963040



Internal ID18598282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35380136..35395888hg38UCSC Ensembl
Innerchr19:35871038..35886790hg19UCSC Ensembl
Innerchr19:40562878..40578630hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3815753
hg1915753
hg1815753
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2146224, nssv2146225, nssv2146228, nssv2146229, nssv2146233, nssv2146230, nssv2146226, nssv2146231, nssv2146227, nssv2146232
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963040
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