A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766466



Internal ID20542326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9344203..9344203hg38UCSC Ensembl
chr6:9344436..9344436hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270418
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766466
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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