A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486060



Internal ID22543973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45988971..45998324hg38UCSC Ensembl
chr20:44617610..44626963hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg389354
hg199354
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5885142
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486060
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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