A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744934



Internal ID20520938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154157000..154212720hg38UCSC Ensembl
chr4:155078152..155133872hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3855721
hg1955721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285321
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744934
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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