A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762222



Internal ID20538082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110473507..110473507hg38UCSC Ensembl
chr6:110794710..110794710hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288683
Samples
Known GenesSLC22A16
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762222
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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