A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968154



Internal ID18603382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:23969189..23980878hg38UCSC Ensembl
Innerchr5:23969298..23980987hg19UCSC Ensembl
Innerchr5:24005055..24016744hg18UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg3811690
hg1911690
hg1811690
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2349761, nssv2349755, nssv2349762, nssv2349754, nssv2349763, nssv2349757, nssv2349760, nssv2349758, nssv2349759, nssv2349756
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)nsv968154
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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