A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4768148



Internal ID20544008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42610869..42610869hg38UCSC Ensembl
chr11:42632419..42632419hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288691
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4768148
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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