A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016399



Internal ID20583439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99189373..99190716hg38UCSC Ensembl
chr13:99841627..99842970hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg381344
hg191344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491766
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016399
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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