A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374598



Internal ID22600267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55197773..55197852hg38UCSC Ensembl
chr18:52865004..52865083hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936404
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374598
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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