A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835991



Internal ID22610926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47008434..47009783hg38UCSC Ensembl
chr3:47049924..47051273hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381350
hg191350
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17492501
Samples
Known GenesNBEAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835991
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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