A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483841



Internal ID21141394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108219467..108220053hg38UCSC Ensembl
chr13:108871815..108872401hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38587
hg19587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006468
Samples
Known GenesABHD13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483841
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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