A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633242



Internal ID21825289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:54124046..54124101hg38UCSC Ensembl
chr18:51650416..51650471hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026054
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633242
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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