A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183547



Internal ID20750587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:62103317..62118079hg38UCSC Ensembl
chr13:62677450..62692212hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3814763
hg1914763
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477549
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183547
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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