A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932282



Internal ID22707577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46060331..46061217hg38UCSC Ensembl
chr13:46634466..46635352hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38887
hg19887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379992
Samples
Known GenesCPB2, CPB2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932282
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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