A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178873



Internal ID20745913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105797601..105833100hg38UCSC Ensembl
chr13:106449950..106485449hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3835500
hg1935500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480964
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178873
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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