A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233696



Internal ID20800736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109095334..109096080hg38UCSC Ensembl
chr8:110107563..110108309hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6434369
Supporting Variants
Samples
Known GenesTRHR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233696
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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