A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743172



Internal ID20519159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63319302..63319363hg38UCSC Ensembl
chr11:63086774..63086835hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285128
Samples
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743172
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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