A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833947



Internal ID22608882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115219135..115220484hg38UCSC Ensembl
chr3:114937982..114939331hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg381350
hg191350
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483793
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833947
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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