A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836287



Internal ID22611222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46616891..46618802hg38UCSC Ensembl
chr3:46658381..46660292hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381912
hg191912
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491555
Samples
Known GenesLOC100132146
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836287
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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