A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865318



Internal ID22640253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68391245..68395144hg38UCSC Ensembl
chr14:68857962..68861861hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455082
Samples
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865318
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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