A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494746



Internal ID21152299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113323556..113366231hg38UCSC Ensembl
chr13:113977871..114020546hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3842676
hg1942676
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185751
Samples
Known GenesGRTP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494746
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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