A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741453



Internal ID20517430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160426571..160426677hg38UCSC Ensembl
chr3:160144359..160144465hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270610
Samples
Known GenesSMC4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741453
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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