A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495199



Internal ID21152752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113913774..113914442hg38UCSC Ensembl
chr13:114616747..114617415hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184566
Samples
Known GenesLINC00452
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495199
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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