A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420688



Internal ID21078241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109112860..109113410hg38UCSC Ensembl
chr8:110125089..110125639hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162842
Samples
Known GenesTRHR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420688
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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