A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485276



Internal ID21142829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68078603..68083637hg38UCSC Ensembl
chr14:68545320..68550354hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg385035
hg195035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020542
Samples
Known GenesRAD51B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485276
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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