A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043688



Internal ID20610728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74215155..74217463hg38UCSC Ensembl
chr18:71882390..71884698hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg382309
hg192309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520076
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043688
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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