A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043920



Internal ID20610960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74591371..74591673hg38UCSC Ensembl
chr18:72258607..72258909hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515750
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043920
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00088


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