A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753534



Internal ID20529394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4895220..4895220hg38UCSC Ensembl
chr6:4895454..4895454hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285335
Samples
Known GenesCDYL
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753534
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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