A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618159



Internal ID21810206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61971519..61971582hg38UCSC Ensembl
chr20:60546575..60546638hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052013
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618159
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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