A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628480



Internal ID21820527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57788034..57788088hg38UCSC Ensembl
chr20:56363090..56363144hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050155
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628480
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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