A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4448582



Internal ID22114759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68136314..68137014hg38UCSC Ensembl
chr14:68603031..68603731hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15756468
Samples
Known GenesRAD51B
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4448582
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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