A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759605



Internal ID20535465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57403441..57403441hg38UCSC Ensembl
chr11:57170914..57170914hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267887
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759605
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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