A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070380



Internal ID21979613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109405138..109405138hg38UCSC Ensembl
chr6:109726341..109726341hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557568
Samples
Known GenesPPIL6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070380
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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