A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965148



Internal ID18600382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22380122..22382866hg38UCSC Ensembl
Innerchr3:22421613..22424357hg19UCSC Ensembl
Innerchr3:22396617..22399361hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382745
hg192745
hg182745
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2273480, nssv2273482, nssv2273479, nssv2273484, nssv2273485, nssv2273486, nssv2273488, nssv2273481, nssv2273483, nssv2273487
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)nsv965148
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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