A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401169



Internal ID21058722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16455881..16464003hg38UCSC Ensembl
chr6:16456112..16464234hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg388123
hg198123
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217000
Samples
Known GenesATXN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401169
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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