A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397065



Internal ID22454935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34200948..34201023hg38UCSC Ensembl
chr20:32788754..32788829hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963852
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397065
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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