A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984022



Internal ID21893365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32319948..32320631hg38UCSC Ensembl
chr1:32785549..32786232hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38684
hg19684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537493
Samples
Known GenesHDAC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984022
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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