A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185483



Internal ID20752523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112953201..112955900hg38UCSC Ensembl
chr13:113607515..113610214hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477404
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185483
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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