A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187774



Internal ID20754814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80334801..80356800hg38UCSC Ensembl
chr10:82094557..82116556hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3822000
hg1922000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448868
Supporting Variants
Samples
Known GenesDYDC1, DYDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187774
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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