A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529690



Internal ID305700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75705464..75716217hg38UCSC Ensembl
chr18:73417419..73428172hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3810754
hg1910754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17719550
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529690
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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