A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179927



Internal ID20746967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99945174..99951858hg38UCSC Ensembl
chr13:100597428..100604112hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg386685
hg196685
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484762
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179927
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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