A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964897



Internal ID18600133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:77540862..77558676hg38UCSC Ensembl
Innerchr5:76836687..76854501hg19UCSC Ensembl
Innerchr5:76872443..76890257hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3817815
hg1917815
hg1817815
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2366374, nssv2366371, nssv2366373, nssv2366367, nssv2366368, nssv2366369, nssv2366372, nssv2366370, nssv2366365, nssv2366366
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)nsv964897
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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