A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476490



Internal ID21134043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28040349..28043134hg38UCSC Ensembl
chr13:28614486..28617271hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg382786
hg192786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007523
Samples
Known GenesFLT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476490
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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