A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978621



Internal ID18613824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:23672035..23673812hg38UCSC Ensembl
Innerchr18:21251999..21253776hg19UCSC Ensembl
Innerchr18:19505997..19507774hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381778
hg191778
hg181778
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2119065, nssv2119067, nssv2119059, nssv2119060, nssv2119066, nssv2119062, nssv2119058, nssv2119063, nssv2119061, nssv2119064
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)nsv978621
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer