A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18013786



Internal ID20580826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:83481273..83484942hg38UCSC Ensembl
chr13:84055408..84059077hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg383670
hg193670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487433
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18013786
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00046


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