A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835643



Internal ID22610578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39958151..39971203hg38UCSC Ensembl
chr3:39999642..40012694hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3813053
hg1913053
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491472
Samples
Known GenesMYRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835643
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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