A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739207



Internal ID20515180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:105663063..105663200hg38UCSC Ensembl
chr3:105381907..105382044hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259379
Samples
Known GenesCBLB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739207
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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