A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475794



Internal ID21133347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113296401..113297800hg38UCSC Ensembl
chr13:113950716..113952115hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187768
Samples
Known GenesLAMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475794
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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