A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764109



Internal ID20539969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30839151..30839151hg38UCSC Ensembl
chr16:30850472..30850472hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294930
Samples
Known GenesBCL7C
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764109
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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