A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18009469



Internal ID20576509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50072062..50072686hg38UCSC Ensembl
chr13:50646198..50646822hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38625
hg19625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6486259
Supporting Variants
Samples
Known GenesDLEU2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18009469
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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