A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014259



Internal ID21923602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117687039..117687160hg38UCSC Ensembl
chr6:118008202..118008323hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559813
Samples
Known GenesNUS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014259
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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