A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715285



Internal ID138951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9036573..9037200hg38UCSC Ensembl
chr18:9036571..9037198hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5526014
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715285
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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