A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837422



Internal ID22612357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87086110..87094581hg38UCSC Ensembl
chr3:87135260..87143731hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg388472
hg198472
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496151
Samples
Known GenesLINC00506
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837422
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer