A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254602



Internal ID20821642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:152144853..152145972hg38UCSC Ensembl
chr2:153001367..153002486hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg381120
hg191120
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553663
Supporting Variants
Samples
Known GenesSTAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254602
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