A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269234



Internal ID20478452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50452027..50452099hg38UCSC Ensembl
chr20:49068564..49068636hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737807
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269234
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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