A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007850



Internal ID20574891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29223666..29233866hg38UCSC Ensembl
chr13:29797803..29808003hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3810201
hg1910201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483059
Supporting Variants
Samples
Known GenesMTUS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007850
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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