A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17483232



Internal ID22541139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18695912..18697511hg38UCSC Ensembl
chr20:18676556..18678155hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877251
Supporting Variants
Samples
Known GenesDTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17483232
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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