A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18124942



Internal ID20691982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:110970396..110972045hg38UCSC Ensembl
chr5:110306095..110307744hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg381650
hg191650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411407
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18124942
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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