A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171882



Internal ID20738922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:99547328..99654773hg38UCSC Ensembl
chr8:100559556..100667001hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38107446
hg19107446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435373
Supporting Variants
Samples
Known GenesVPS13B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171882
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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