A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253936



Internal ID20820976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8545849..8546603hg38UCSC Ensembl
chr1:8605908..8606662hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38755
hg19755
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535613
Supporting Variants
Samples
Known GenesRERE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253936
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00022


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