A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195962



Internal ID20763002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91332901..91354100hg38UCSC Ensembl
chr13:91985155..92006354hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3821200
hg1921200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6478645
Supporting Variants
Samples
Known GenesMIR17, MIR17HG, MIR18A, MIR19A, MIR19B1, MIR20A, MIR92A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195962
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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