A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480091



Internal ID21137644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40586473..40587182hg38UCSC Ensembl
chr13:41160610..41161319hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38710
hg19710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008909
Samples
Known GenesFOXO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480091
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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