A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579846



Internal ID20952917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69220480..69222083hg38UCSC Ensembl
chr14:69687197..69688800hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg381604
hg191604
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237941
Samples
Known GenesEXD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579846
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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