A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968879



Internal ID18604107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17353511..17359035hg38UCSC Ensembl
Innerchr5:17353620..17359144hg19UCSC Ensembl
Innerchr5:17406620..17412144hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg385525
hg195525
hg185525
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2347370, nssv2347374, nssv2347365, nssv2347366, nssv2347373, nssv2347372, nssv2347367, nssv2347368, nssv2347369, nssv2347371
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)nsv968879
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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