A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460803



Internal ID22518686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206641297..206642491hg38UCSC Ensembl
chr1:206814642..206815836hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381195
hg191195
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829170
Supporting Variants
Samples
Known GenesDYRK3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460803
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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