A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877299



Internal ID22652263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151760899..151761449hg38UCSC Ensembl
chr1:151733375..151733925hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357051
Samples
Known GenesMRPL9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877299
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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