A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264229



Internal ID20831269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158909973..158910282hg38UCSC Ensembl
chr4:159831125..159831434hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557291
Supporting Variants
Samples
Known GenesC4orf45
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264229
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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