A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292425



Internal ID20501643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33093540..33093644hg38UCSC Ensembl
chr20:31681346..31681450hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736510
Supporting Variants
Samples
Known GenesBPIFB4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292425
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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