A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971670



Internal ID18260201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:78747500..78767593hg38UCSC Ensembl
Innerchr8:79659735..79679828hg19UCSC Ensembl
Innerchr8:79822290..79842383hg18UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3820094
hg1920094
hg1820094
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2510123, nssv2510127, nssv2508824, nssv2510126, nssv2510122, nssv2508823, nssv2510121, nssv2510124, nssv2510120, nssv2510125
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesIL7
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971670
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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