A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486075



Internal ID22543988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47449125..47453747hg38UCSC Ensembl
chr20:46077869..46082491hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg384623
hg194623
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5887045
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486075
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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