A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515258



Internal ID291741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:72323938..72381499hg38UCSC Ensembl
chr18:69991173..70048734hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3857562
hg1957562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17719371
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515258
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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