A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17717920



Internal ID141586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:46837168..46837350hg38UCSC Ensembl
chr18:44417131..44417313hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513923
Supporting Variants
Samples
Known GenesPIAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17717920
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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