A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978616



Internal ID18613819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14878824..14883874hg38UCSC Ensembl
Innerchr18:14878823..14883873hg19UCSC Ensembl
Innerchr18:14868823..14873873hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg385051
hg195051
hg185051
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2118787, nssv2118782, nssv2118783, nssv2118788, nssv2118789, nssv2118781, nssv2118780, nssv2118785, nssv2118784, nssv2118786
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)nsv978616
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