A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926928



Internal ID22702156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112208477..112210459hg38UCSC Ensembl
chr9:114970757..114972739hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381983
hg191983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439829
Samples
Known GenesMIR3134
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926928
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