A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558323



Internal ID20931394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124047375..124048589hg38UCSC Ensembl
chr8:125059616..125060830hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg381215
hg191215
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276135
Samples
Known GenesFER1L6, FER1L6-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558323
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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