A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835198



Internal ID22610133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196496121..196497720hg38UCSC Ensembl
chr3:196222992..196224591hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490436
Samples
Known GenesRNF168
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835198
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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