A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988735



Internal ID21898078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239303895..239307343hg38UCSC Ensembl
chr2:240225590..240229038hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg383449
hg193449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535655
Samples
Known GenesHDAC4, MIR4269
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988735
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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