A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733147



Internal ID20509074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112398038..112398376hg38UCSC Ensembl
chr10:114157796..114158134hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286942
Samples
Known GenesACSL5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733147
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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