A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182804



Internal ID20749844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96517053..96573574hg38UCSC Ensembl
chr13:97169307..97225828hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3856522
hg1956522
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489293
Supporting Variants
Samples
Known GenesHS6ST3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182804
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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