A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248872



Internal ID20815912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1807480..1807674hg38UCSC Ensembl
chr1:1738919..1739113hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552922
Supporting Variants
Samples
Known GenesGNB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248872
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