A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482588



Internal ID22540493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14193674..14219885hg38UCSC Ensembl
chr20:14174320..14200531hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3826212
hg1926212
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881019
Supporting Variants
Samples
Known GenesMACROD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482588
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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