A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981895



Internal ID18617091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:60001..67190hg38UCSC Ensembl
Innerchr8:10001..17190hg19UCSC Ensembl
Innerchr8:1..7190hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg387190
hg197190
hg187190
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2490343, nssv2490340, nssv2490344, nssv2490347, nssv2490342, nssv2490345, nssv2490349, nssv2490346, nssv2490348, nssv2490341
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)nsv981895
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