A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913279



Internal ID22688495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73249890..73250022hg38UCSC Ensembl
chr10:75009648..75009780hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357851
Samples
Known GenesDNAJC9-AS1, MRPS16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913279
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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