A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980830



Internal ID18616030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181331295..181333704hg38UCSC Ensembl
Innerchr5:180758296..180760705hg19UCSC Ensembl
Innerchr5:180690902..180693311hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg382410
hg192410
hg182410
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2704168, nssv2704166, nssv2704162, nssv2704165, nssv2704169, nssv2704161, nssv2704163, nssv2704167, nssv2704160, nssv2704164
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv980830
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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