A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760190



Internal ID20536050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130193783..130193783hg38UCSC Ensembl
chr11:130063678..130063678hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267290
Samples
Known GenesST14
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760190
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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