A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18120785



Internal ID20687825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94735999..94738792hg38UCSC Ensembl
chr4:95657150..95659943hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg382794
hg192794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383203
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18120785
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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