A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913848



Internal ID22689064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112884573..112890104hg38UCSC Ensembl
chr9:115646853..115652384hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg385532
hg195532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433540
Samples
Known GenesSLC46A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913848
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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