A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147218



Internal ID346400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91051777..91052212hg38UCSC Ensembl
chr14:91518121..91518556hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17697226
Samples
Known GenesRPS6KA5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147218
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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