A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743103



Internal ID20519089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:117910278..117910465hg38UCSC Ensembl
chr3:117629125..117629312hg19UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296203
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743103
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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