A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556518



Internal ID20929589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109466531..109467180hg38UCSC Ensembl
chr4:110387687..110388336hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262988
Samples
Known GenesSEC24B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556518
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