A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18106319



Internal ID20673359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:113940901..113943000hg38UCSC Ensembl
chr4:114862057..114864156hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381704
Supporting Variants
Samples
Known GenesARSJ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18106319
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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