A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18041333



Internal ID20608373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:40048581..40050937hg38UCSC Ensembl
chr18:37628545..37630901hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg382357
hg192357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535416
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18041333
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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