A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17462883



Internal ID22520768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206641296..206642297hg38UCSC Ensembl
chr1:206814641..206815642hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829169
Supporting Variants
Samples
Known GenesDYRK3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17462883
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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