A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279807



Internal ID20846847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123645917..123646889hg38UCSC Ensembl
chr9:126408196..126409168hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38973
hg19973
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573973
Supporting Variants
Samples
Known GenesDENND1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279807
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