A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249591



Internal ID20816631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:18914043..18914618hg38UCSC Ensembl
chr1:19240537..19241112hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539820
Supporting Variants
Samples
Known GenesIFFO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249591
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