A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287238



Internal ID20496456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31689247..31689247hg38UCSC Ensembl
chr20:30277050..30277050hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758264
Supporting Variants
Samples
Known GenesBCL2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287238
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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