A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187332



Internal ID20754372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118693254..119214513hg38UCSC Ensembl
chr10:120452766..120974025hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38521260
hg19521260
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450643
Supporting Variants
Samples
Known GenesCACUL1, EIF3A, FAM45A, FAM45B, GRK5, NANOS1, PRDX3, SFXN4, SNORA19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187332
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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