A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18111093



Internal ID20678133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158046451..158046626hg38UCSC Ensembl
chr4:158967603..158967778hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392763
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18111093
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01059


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