A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162840



Internal ID20729881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109091303..109095968hg38UCSC Ensembl
chr8:110103532..110108197hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg384666
hg194666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430424
Supporting Variants
Samples
Known GenesTRHR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162840
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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