A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893853



Internal ID22668919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:38879445..38879518hg38UCSC Ensembl
chr5:38879547..38879620hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412524
Samples
Known GenesOSMR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893853
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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