A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981174



Internal ID18616373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:111430113..111431817hg38UCSC Ensembl
Innerchr6:111751316..111753020hg19UCSC Ensembl
Innerchr6:111858009..111859713hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381705
hg191705
hg181705
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2419829, nssv2419832, nssv2419831, nssv2419833, nssv2419835, nssv2419834, nssv2419828, nssv2419836, nssv2419830, nssv2419827
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesREV3L
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981174
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