A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18013922



Internal ID20580962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:82713341..82713861hg38UCSC Ensembl
chr13:83287476..83287996hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6482276
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18013922
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00032


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