A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18009465



Internal ID20576505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50018910..50031605hg38UCSC Ensembl
chr13:50593046..50605741hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3812696
hg1912696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490437
Supporting Variants
Samples
Known GenesDLEU2, KCNRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18009465
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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