A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852629



Internal ID22627564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115429383..115433066hg38UCSC Ensembl
chr8:116441611..116445294hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg383684
hg193684
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505585
Samples
Known GenesTRPS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852629
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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