A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836662



Internal ID22611597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51736781..51739483hg38UCSC Ensembl
chr3:51770797..51773499hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg382703
hg192703
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493225
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836662
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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