A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581795



Internal ID20954866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68441344..68831278hg38UCSC Ensembl
chr14:68908061..69297995hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38389935
hg19389935
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237923
Samples
Known GenesRAD51B, ZFP36L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581795
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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