A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18013550



Internal ID20580590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80410402..80410817hg38UCSC Ensembl
chr13:80984537..80984952hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38416
hg19416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6478033
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18013550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00138


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