A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012098



Internal ID21921441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115539134..115539626hg38UCSC Ensembl
chr8:116551361..116551853hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583371
Samples
Known GenesTRPS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012098
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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