A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481885



Internal ID21139438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102334769..102335337hg38UCSC Ensembl
chr13:102987119..102987687hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006369
Samples
Known GenesFGF14, FGF14-IT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481885
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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