A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050074



Internal ID21959307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28158705..28158705hg38UCSC Ensembl
chr1:28485216..28485216hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg382365
hg192365
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525484
Samples
Known GenesPTAFR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050074
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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