A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264036



Internal ID20473254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:53868473..53868580hg38UCSC Ensembl
chr2:54095610..54095717hg19UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739437
Supporting Variants
Samples
Known GenesPSME4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264036
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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