A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592941



Internal ID20966012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67234685..67234991hg38UCSC Ensembl
chr14:67701402..67701708hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592941
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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