A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524594



Internal ID300795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76139876..76139999hg38UCSC Ensembl
chr18:73851831..73851954hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17719575
Samples
Known GenesLOC339298
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524594
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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