A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619476



Internal ID21811523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21065054..21065916hg38UCSC Ensembl
chr20:21045695..21046557hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38863
hg19863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050954
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619476
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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