A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620047



Internal ID21812094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60256530..60256969hg38UCSC Ensembl
chr20:58831588..58832027hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042461
Supporting Variants
Samples
Known GenesLOC284757
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620047
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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