A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295226



Internal ID20504444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:169079903..169079988hg38UCSC Ensembl
chr2:169936413..169936498hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743654
Supporting Variants
Samples
Known GenesDHRS9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295226
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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