A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890699



Internal ID22665727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:54709888..54715451hg38UCSC Ensembl
chr5:54005716..54011279hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg385564
hg195564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411817
Samples
Known GenesLOC102467080
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890699
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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