A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293521



Internal ID20502739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18209143..18209640hg38UCSC Ensembl
chr20:18189787..18190284hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743363
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293521
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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