A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966987



Internal ID18602216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:9348169..9349971hg38UCSC Ensembl
Innerchr3:9389853..9391655hg19UCSC Ensembl
Innerchr3:9364853..9366655hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg381803
hg191803
hg181803
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2273717, nssv2273715, nssv2273720, nssv2273718, nssv2273723, nssv2273722, nssv2273721, nssv2273719, nssv2273724, nssv2273716
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)nsv966987
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