A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836811



Internal ID22611746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:76550735..76552384hg38UCSC Ensembl
chr3:76599886..76601535hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg381650
hg191650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495385, nssv17495384
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836811
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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