A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965152



Internal ID18600386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32186231..32193084hg38UCSC Ensembl
Innerchr3:32227723..32234576hg19UCSC Ensembl
Innerchr3:32202727..32209580hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg386854
hg196854
hg186854
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2274108, nssv2274113, nssv2274110, nssv2273578, nssv2274109, nssv2273579, nssv2274111, nssv2273577, nssv2274112, nssv2273576
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)nsv965152
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