A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18113807



Internal ID20680847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17890699..17893166hg38UCSC Ensembl
chr4:17892322..17894789hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg382468
hg192468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360522
Supporting Variants
Samples
Known GenesLCORL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18113807
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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