A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715207



Internal ID138873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3335854..3337332hg38UCSC Ensembl
chr18:3335852..3337330hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381479
hg191479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520882
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715207
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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