A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485466



Internal ID21143019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105691897..105692433hg38UCSC Ensembl
chr13:106344246..106344782hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006780
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485466
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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