A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173611



Internal ID20740651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:99159093..99251631hg38UCSC Ensembl
chr8:100171321..100263859hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3892539
hg1992539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417613
Supporting Variants
Samples
Known GenesVPS13B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173611
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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