A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234058



Internal ID20801098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28570981..28572331hg38UCSC Ensembl
chr10:28859910..28861260hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg381351
hg191351
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578485
Supporting Variants
Samples
Known GenesWAC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234058
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