A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423403



Internal ID21080956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93192546..93192914hg38UCSC Ensembl
chr8:94204775..94205143hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171731
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423403
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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