A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007274



Internal ID20574314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108076560..108081294hg38UCSC Ensembl
chr13:108728908..108733642hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg384735
hg194735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487444
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007274
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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