A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18252725



Internal ID20819765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92844958..92845509hg38UCSC Ensembl
chr1:93310515..93311066hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550244
Supporting Variants
Samples
Known GenesFAM69A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18252725
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