A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859064



Internal ID22633999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115451510..115454845hg38UCSC Ensembl
chr8:116463738..116467073hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg383336
hg193336
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505594
Samples
Known GenesTRPS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859064
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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