A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162619



Internal ID20729659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10337476..10339735hg38UCSC Ensembl
chr8:10194986..10197245hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg382260
hg192260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433797
Supporting Variants
Samples
Known GenesMSRA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162619
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00057


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