A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748557



Internal ID20524584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134138342..134138786hg38UCSC Ensembl
chr11:134008237..134008681hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265727
Samples
Known GenesJAM3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748557
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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