A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493046



Internal ID21150599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68354526..68357813hg38UCSC Ensembl
chr14:68821243..68824530hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg383288
hg193288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020563
Samples
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493046
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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