A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744732



Internal ID20520734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129945056..129945138hg38UCSC Ensembl
chr10:131743320..131743402hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16262047
Samples
Known GenesEBF3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744732
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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