A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17717292



Internal ID140958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35179936..35187871hg38UCSC Ensembl
chr18:32759900..32767835hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg387936
hg197936
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516528
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17717292
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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