A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968128



Internal ID18603356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181371476..181438401hg38UCSC Ensembl
Innerchr5:180798477..180865402hg19UCSC Ensembl
Innerchr5:180731083..180798008hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3866926
hg1966926
hg1866926
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2392554, nssv2392552, nssv2392550, nssv2392553, nssv2392559, nssv2392558, nssv2392555, nssv2392557, nssv2392556, nssv2392551
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)nsv968128
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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