A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456369



Internal ID234439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183722299..183724312hg38UCSC Ensembl
chr4:184643452..184645465hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg382014
hg192014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16959710
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456369
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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