A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277522



Internal ID20486740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5027677..5027942hg38UCSC Ensembl
chr20:5008323..5008588hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735155
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277522
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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