A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18113272



Internal ID20680312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20715214..20718793hg38UCSC Ensembl
chr4:20716837..20720416hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg383580
hg193580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368431
Supporting Variants
Samples
Known GenesPACRGL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18113272
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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