A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484248



Internal ID21141801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68369807..68374768hg38UCSC Ensembl
chr14:68836524..68841485hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg384962
hg194962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020565
Samples
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484248
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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