A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490437



Internal ID21147990
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 StatusM
Merged Variants
Supporting Variantsnssv18009465
Samples
Known GenesDLEU2, KCNRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490437
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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