A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18041057



Internal ID20608097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:43776482..43785462hg38UCSC Ensembl
chr18:41356447..41365427hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg388981
hg198981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533970
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18041057
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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