A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968136



Internal ID18603364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1639971..1640971hg38UCSC Ensembl
Innerchr5:1640086..1641086hg19UCSC Ensembl
Innerchr5:1693086..1694086hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2346530, nssv2346531, nssv2346529, nssv2346527, nssv2346534, nssv2346532, nssv2346528, nssv2346526, nssv2346535, nssv2346533
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)nsv968136
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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