A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262725



Internal ID20471943
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 StatusS
Merged Variantsnsv4745936
Supporting Variants
Samples
Known GenesHDAC4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262725
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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