A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963308



Internal ID18598549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:33076461..33079559hg38UCSC Ensembl
Innerchr3:33117953..33121051hg19UCSC Ensembl
Innerchr3:33092957..33096055hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg383099
hg193099
hg183099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2277049, nssv2277054, nssv2277051, nssv2277047, nssv2277048, nssv2277055, nssv2277053, nssv2277050, nssv2277052, nssv2277046
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGLB1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963308
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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