A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978612



Internal ID18613815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14605815..14665770hg38UCSC Ensembl
Innerchr18:14605814..14665769hg19UCSC Ensembl
Innerchr18:14595814..14655769hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3859956
hg1959956
hg1859956
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2118284, nssv2118283, nssv2118276, nssv2118275, nssv2118280, nssv2118278, nssv2118281, nssv2118279, nssv2118277, nssv2118282
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)nsv978612
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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