A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452937



Internal ID231079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18692458..18694737hg38UCSC Ensembl
chr4:18694081..18696360hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg382280
hg192280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16948358
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452937
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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