A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18113381



Internal ID20680421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24991341..24993658hg38UCSC Ensembl
chr4:24992963..24995280hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg382318
hg192318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373720
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18113381
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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