A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451158



Internal ID21108711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113261244..113264209hg38UCSC Ensembl
chr9:116023524..116026489hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg382966
hg192966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174382
Samples
Known GenesSLC31A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451158
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer