A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428452



Internal ID21086005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93168547..93174992hg38UCSC Ensembl
chr8:94180776..94187221hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg386446
hg196446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171729
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428452
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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