A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061834



Internal ID21971067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108232858..108232858hg38UCSC Ensembl
chr6:108554062..108554062hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560743
Samples
Known GenesSNX3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061834
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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