A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731428



Internal ID20507349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1828115..1829059hg38UCSC Ensembl
chr4:1829842..1830786hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38945
hg19945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274081
Samples
Known GenesLETM1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731428
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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