A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539751



Internal ID20913046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23911293..23912017hg38UCSC Ensembl
chr3:23952784..23953508hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38725
hg19725
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261992
Samples
Known GenesNKIRAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539751
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