A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429167



Internal ID21086720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20682636..20686022hg38UCSC Ensembl
chr8:20540147..20543533hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg383387
hg193387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166010
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429167
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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