A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618282



Internal ID21810329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:40103467..40103631hg38UCSC Ensembl
chr18:37683431..37683595hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034824
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618282
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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