A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892294



Internal ID22667342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55183563..55184044hg38UCSC Ensembl
chr5:54479391..54479872hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428596
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892294
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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