A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253479



Internal ID20820519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:12656947..12910448hg38UCSC Ensembl
chr20:12637594..12891096hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38253502
hg19253503
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596002
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253479
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00013


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