A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044341



Internal ID20611381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8993087..9004561hg38UCSC Ensembl
chr18:8993085..9004559hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3811475
hg1911475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534548
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044341
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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