A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402477



Internal ID22460347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21270453..21271103hg38UCSC Ensembl
chr20:21251091..21251741hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954176
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402477
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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