A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18009067



Internal ID20576109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:43281500..43284361hg38UCSC Ensembl
chr13:43855636..43858497hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg382862
hg192862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488326
Supporting Variants
Samples
Known GenesENOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18009067
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00455


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