A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835553



Internal ID22610488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24058489..24083754hg38UCSC Ensembl
chr3:24099980..24125245hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3825266
hg1925266
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490538
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835553
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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