A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836286



Internal ID22611221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46521988..46528779hg38UCSC Ensembl
chr3:46563478..46570269hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg386792
hg196792
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491554
Samples
Known GenesLRRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836286
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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