A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17528546



Internal ID21852903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:49744534..49750113hg38UCSC Ensembl
chr2:49971672..49977251hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg385580
hg195580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989441
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17528546
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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