A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476050



Internal ID21133603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101452301..101455900hg38UCSC Ensembl
chr13:102104652..102108251hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186774
Samples
Known GenesITGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476050
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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