A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852263



Internal ID22627198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18894143..18930204hg38UCSC Ensembl
chr8:18751653..18787714hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3836062
hg1936062
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505082
Samples
Known GenesPSD3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852263
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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