A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18057098



Internal ID20624138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206646201..206650100hg38UCSC Ensembl
chr1:206819546..206823445hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318975
Supporting Variants
Samples
Known GenesDYRK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18057098
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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