A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586623



Internal ID20959694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93244585..93244957hg38UCSC Ensembl
chr14:93710931..93711303hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238357
Samples
Known GenesBTBD7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586623
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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