A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835512



Internal ID22610447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194822494..194825493hg38UCSC Ensembl
chr3:194543223..194546222hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835512
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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