A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052123



Internal ID21961356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43184923..43184923hg38UCSC Ensembl
chr1:43650594..43650594hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531546
Samples
Known GenesWDR65
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052123
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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