A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744816



Internal ID20520819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:90205009..90205244hg38UCSC Ensembl
chr3:90254159..90254394hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282587
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744816
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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