A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183159



Internal ID20750199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103903901..103965700hg38UCSC Ensembl
chr13:104556251..104618050hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3861800
hg1961800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6478343
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183159
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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