A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17528665



Internal ID21853022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238269504..238269591hg38UCSC Ensembl
chr2:239178145..239178232hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5988238
Supporting Variants
Samples
Known GenesPER2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17528665
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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