A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008910



Internal ID20575952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40594983..40595664hg38UCSC Ensembl
chr13:41169120..41169801hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38682
hg19682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475790
Supporting Variants
Samples
Known GenesFOXO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008910
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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