A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275992



Internal ID20843032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44671487..44672656hg38UCSC Ensembl
chr7:44711086..44712255hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg381170
hg191170
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573886
Supporting Variants
Samples
Known GenesOGDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275992
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