A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910787



Internal ID22685998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74832789..74838426hg38UCSC Ensembl
chr9:77447705..77453342hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg385638
hg195638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434835
Samples
Known GenesTRPM6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910787
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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