A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18164038



Internal ID20731078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123973203..123987488hg38UCSC Ensembl
chr8:124985443..124999728hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3814286
hg1914286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416274
Supporting Variants
Samples
Known GenesFER1L6, FER1L6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18164038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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