A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968889



Internal ID18604117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:20799436..20857594hg38UCSC Ensembl
Innerchr5:20799545..20857703hg19UCSC Ensembl
Innerchr5:20835302..20893460hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3858159
hg1958159
hg1858159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2349096, nssv2349101, nssv2349099, nssv2349098, nssv2349102, nssv2349095, nssv2349093, nssv2349094, nssv2349100, nssv2349097
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)nsv968889
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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