A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981962



Internal ID18617158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:86041819..86044239hg38UCSC Ensembl
Innerchr8:87054048..87056468hg19UCSC Ensembl
Innerchr8:87123164..87125584hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg382421
hg192421
hg182421
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2510394, nssv2512493, nssv2510393, nssv2510395, nssv2512494, nssv2512496, nssv2510390, nssv2510391, nssv2512495, nssv2510392
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)nsv981962
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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