A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488017



Internal ID21145570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108220121..108220614hg38UCSC Ensembl
chr13:108872469..108872962hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38494
hg19494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006469
Samples
Known GenesABHD13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488017
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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