A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836773



Internal ID22611708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68993325..68994596hg38UCSC Ensembl
chr3:69042476..69043747hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381272
hg191272
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494683
Samples
Known GenesEOGT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836773
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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