A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984044



Internal ID21893387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35640584..35640692hg38UCSC Ensembl
chr1:36106185..36106293hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535569
Samples
Known GenesPSMB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984044
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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