A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064432



Internal ID21973665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106258501..106258501hg38UCSC Ensembl
chr6:106706376..106706376hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382569
hg192569
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577145
Samples
Known GenesATG5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064432
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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