A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17719552



Internal ID143218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75741824..75769586hg38UCSC Ensembl
chr18:73453779..73481541hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3827763
hg1927763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522805
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17719552
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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