A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494472



Internal ID21152025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28051794..28052344hg38UCSC Ensembl
chr13:28625931..28626481hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007524
Samples
Known GenesFLT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494472
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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