A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980771



Internal ID18615971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179931286..179933938hg38UCSC Ensembl
Innerchr5:179358286..179360938hg19UCSC Ensembl
Innerchr5:179290892..179293544hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg382653
hg192653
hg182653
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2390307, nssv2390312, nssv2390310, nssv2390313, nssv2390309, nssv2390308, nssv2390311, nssv2390314, nssv2390315, nssv2390316
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)nsv980771
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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