A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741143



Internal ID20517120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155498414..155498528hg38UCSC Ensembl
chr4:156419566..156419680hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268804
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741143
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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