A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962489



Internal ID18597732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11920675..11929410hg38UCSC Ensembl
Innerchr18:11920674..11929409hg19UCSC Ensembl
Innerchr18:11910674..11919409hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg388736
hg198736
hg188736
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2114570, nssv2114571, nssv2114576, nssv2114568, nssv2114575, nssv2114574, nssv2114572, nssv2114567, nssv2114573, nssv2114569
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)nsv962489
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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