A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190381



Internal ID20757421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109766801..109908600hg38UCSC Ensembl
chr13:110419148..110560947hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38141800
hg19141800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487821
Supporting Variants
Samples
Known GenesIRS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190381
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00031


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