A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17486073



Internal ID22543986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4737516..4740015hg38UCSC Ensembl
chr20:4718162..4720661hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875572
Supporting Variants
Samples
Known GenesPRNT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17486073
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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