A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738123



Internal ID20514090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26384768..26384908hg38UCSC Ensembl
chr4:26386390..26386530hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275605
Samples
Known GenesRBPJ
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738123
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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