A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18040344



Internal ID20607384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22924601..22933300hg38UCSC Ensembl
chr18:20504564..20513263hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532511
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18040344
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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