A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979806



Internal ID18615007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:15121347..15146636hg38UCSC Ensembl
Innerchr3:15162854..15188143hg19UCSC Ensembl
Innerchr3:15137858..15163147hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3825290
hg1925290
hg1825290
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2274623, nssv2274620, nssv2274618, nssv2274616, nssv2274621, nssv2274619, nssv2274622, nssv2274615, nssv2274617, nssv2274624
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)nsv979806
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