A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560058



Internal ID20933129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:167282036..168440434hg38UCSC Ensembl
chr4:168203187..169361585hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg381158399
hg191158399
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264334
Samples
Known GenesANXA10, DDX60, DDX60L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560058
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