A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18013682



Internal ID20580722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:78972943..78973543hg38UCSC Ensembl
chr13:79547078..79547678hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487382
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18013682
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00034


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