A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576438



Internal ID21524877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115534212..115534316hg38UCSC Ensembl
chr8:116546439..116546543hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155051
SamplesHG01505
Known GenesTRPS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5576438
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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