A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767743



Internal ID20543603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117924186..117924186hg38UCSC Ensembl
chr11:117794901..117794901hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265227
Samples
Known GenesTMPRSS13
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767743
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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