A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766600



Internal ID20542460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123593659..123593659hg38UCSC Ensembl
chr6:123914804..123914804hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288188
Samples
Known GenesTRDN
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766600
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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