A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920151



Internal ID22695374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34518759..34518928hg38UCSC Ensembl
chr9:34518757..34518926hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434538
Samples
Known GenesDNAI1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920151
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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