A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016752



Internal ID21926095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112913988..112914089hg38UCSC Ensembl
chr5:112249685..112249786hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539089
Samples
Known GenesREEP5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016752
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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