A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17557568



Internal ID21881923
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 StatusS
Merged Variantsnsv6070380
Supporting Variants
Samples
Known GenesPPIL6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17557568
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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