A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18013360



Internal ID20580400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75570078..75570645hg38UCSC Ensembl
chr13:76144214..76144781hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38568
hg19568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487262
Supporting Variants
Samples
Known GenesUCHL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18013360
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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