A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179289



Internal ID20746329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56505735..56635744hg38UCSC Ensembl
chr18:54172966..54302975hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38130010
hg19130010
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533679
Supporting Variants
Samples
Known GenesTXNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179289
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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