A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17487314



Internal ID22545230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62506752..62538568hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3831817
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878227
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17487314
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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