A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759416



Internal ID20535276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44663557..44663557hg38UCSC Ensembl
chr11:44685107..44685107hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284980
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759416
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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