A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068346



Internal ID21977579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105825617..105825617hg38UCSC Ensembl
chr7:105466063..105466063hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570376
Samples
Known GenesATXN7L1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068346
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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