A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745936



Internal ID20521947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239231621..239231832hg38UCSC Ensembl
chr2:240153317..240153528hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262725
Samples
Known GenesHDAC4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745936
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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