A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17632826



Internal ID21824873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19273724..19273842hg38UCSC Ensembl
chr20:19254368..19254486hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6047955
Supporting Variants
Samples
Known GenesLOC100130264, SLC24A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17632826
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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