A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17718643



Internal ID142309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:60467903..60483298hg38UCSC Ensembl
chr18:58135136..58150531hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3815396
hg1915396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144757
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17718643
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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