A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585900



Internal ID20958971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58422861..58423479hg38UCSC Ensembl
chr14:58889579..58890197hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38619
hg19619
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237903
Samples
Known GenesTIMM9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585900
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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