A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18005937



Internal ID20572977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102882885..102883797hg38UCSC Ensembl
chr13:103535235..103536147hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38913
hg19913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487603
Supporting Variants
Samples
Known GenesMETTL21EP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18005937
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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