A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004163



Internal ID21913506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125005584..125022685hg38UCSC Ensembl
chr6:125326730..125343831hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3817102
hg1917102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564180
Samples
Known GenesRNF217
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004163
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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