A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761590



Internal ID20537450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13016499..13016499hg38UCSC Ensembl
chr11:13038046..13038046hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761590
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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