A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067187



Internal ID21976420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140781628..140781628hg38UCSC Ensembl
chr8:141791727..141791727hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594449
Samples
Known GenesPTK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067187
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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