A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974825



Internal ID18610034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:68713358..68721616hg38UCSC Ensembl
Innerchr16:68747261..68755519hg19UCSC Ensembl
Innerchr16:67304762..67313020hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg388259
hg198259
hg188259
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2065342, nssv2065340, nssv2065345, nssv2065339, nssv2065347, nssv2065346, nssv2065344, nssv2065343, nssv2065341, nssv2065348
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)nsv974825
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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