A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740345



Internal ID20516320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:111501698..111505081hg38UCSC Ensembl
chr4:112422854..112426237hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg383384
hg193384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280612
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740345
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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