A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18163545



Internal ID20730585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:112323688..112324341hg38UCSC Ensembl
chr8:113335917..113336570hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432879
Supporting Variants
Samples
Known GenesCSMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18163545
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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