A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283407



Internal ID20492625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132496825..132496929hg38UCSC Ensembl
chr12:133073411..133073515hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746227
Supporting Variants
Samples
Known GenesFBRSL1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283407
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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