A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493301



Internal ID21150854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113593330..113594467hg38UCSC Ensembl
chr13:114247645..114248782hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381138
hg191138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007776
Samples
Known GenesTFDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493301
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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