A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967009



Internal ID18602238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:44573956..44577610hg38UCSC Ensembl
Innerchr3:44615448..44619102hg19UCSC Ensembl
Innerchr3:44590452..44594106hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg383655
hg193655
hg183655
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2279411, nssv2279406, nssv2279405, nssv2279410, nssv2279404, nssv2279407, nssv2279408, nssv2279403, nssv2279412, nssv2279409
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZKSCAN7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967009
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