A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837114



Internal ID22612049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78328665..78354560hg38UCSC Ensembl
chr3:78377815..78403710hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3825896
hg1925896
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495429
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837114
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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