A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476422



Internal ID21133975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113105770..113147336hg38UCSC Ensembl
chr13:113760084..113801650hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3841567
hg1941567
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181903
Samples
Known GenesF10, F7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476422
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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