A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980775



Internal ID18615975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181438401..181461494hg38UCSC Ensembl
Innerchr5:180865402..180888495hg19UCSC Ensembl
Innerchr5:180798008..180821101hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3823094
hg1923094
hg1823094
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2392613, nssv2392615, nssv2392616, nssv2392612, nssv2392608, nssv2392610, nssv2392614, nssv2392611, nssv2392617, nssv2392609
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)nsv980775
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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