A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578732



Internal ID20951803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74769271..74770126hg38UCSC Ensembl
chr14:75235974..75236829hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38856
hg19856
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237279
Samples
Known GenesYLPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578732
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer