A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582899



Internal ID20955970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75143088..75143757hg38UCSC Ensembl
chr14:75609791..75610460hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237296
Samples
Known GenesTMED10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582899
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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