A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482599



Internal ID22540505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14298214..14341700hg38UCSC Ensembl
chr20:14278860..14322346hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3843487
hg1943487
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882936
Supporting Variants
Samples
Known GenesFLRT3, MACROD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482599
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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