A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737406



Internal ID20513367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152111572..152111630hg38UCSC Ensembl
chr4:153032724..153032782hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295475
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737406
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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