A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966988



Internal ID18602217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:9993448..9996549hg38UCSC Ensembl
Innerchr3:10035132..10038233hg19UCSC Ensembl
Innerchr3:10010132..10013233hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg383102
hg193102
hg183102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2270853, nssv2270855, nssv2270858, nssv2270850, nssv2270857, nssv2270856, nssv2270851, nssv2270854, nssv2270852, nssv2270859
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesEMC3-AS1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966988
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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