A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053362



Internal ID20620402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:170089146..170255361hg38UCSC Ensembl
chr1:170058287..170224502hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38166216
hg19166216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333648
Supporting Variants
Samples
Known GenesMETTL11B, MIR3119-1, MIR3119-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053362
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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