A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715358



Internal ID139024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10134500..10145000hg38UCSC Ensembl
chr18:10134497..10144997hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3810501
hg1910501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530429
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715358
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00203


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