A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063369



Internal ID21972602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105664575..105664575hg38UCSC Ensembl
chr7:105305022..105305022hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572309
Samples
Known GenesATXN7L1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063369
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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