A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960265



Internal ID18595518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14984975..14991120hg38UCSC Ensembl
Innerchr18:14984974..14991119hg19UCSC Ensembl
Innerchr18:14974974..14981119hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg386146
hg196146
hg186146
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2118291, nssv2118287, nssv2118294, nssv2118289, nssv2118293, nssv2118295, nssv2119593, nssv2118292, nssv2118290, nssv2118288
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)nsv960265
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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