A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190326



Internal ID20757366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123874191..123889869hg38UCSC Ensembl
chr10:125633707..125649385hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3815679
hg1915679
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447589
Supporting Variants
Samples
Known GenesCPXM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190326
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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