A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746478



Internal ID20522492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239176284..239176367hg38UCSC Ensembl
chr2:240097980..240098063hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263569
Samples
Known GenesHDAC4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746478
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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