A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910768



Internal ID22685979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132666814..132668674hg38UCSC Ensembl
chr9:135542201..135544061hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381861
hg191861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443015
Samples
Known GenesDDX31
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910768
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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