A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121296



Internal ID20688336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99082153..99084963hg38UCSC Ensembl
chr4:100003304..100006114hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg382811
hg192811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380422
Supporting Variants
Samples
Known GenesADH5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121296
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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