A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171505



Internal ID20738545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89508322..89584273hg38UCSC Ensembl
chr8:90520551..90596502hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3875952
hg1975952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429789
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171505
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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