A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633128



Internal ID21825175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:54305498..54305682hg38UCSC Ensembl
chr18:51831868..51832052hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025733
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633128
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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