A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486017



Internal ID22543930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4290242..4293874hg38UCSC Ensembl
chr20:4270889..4274521hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383633
hg193633
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871601
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486017
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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