A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257009



Internal ID20824049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191558937..191559398hg38UCSC Ensembl
chr2:192423663..192424124hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538064
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257009
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0005


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