A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062798



Internal ID21972031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168309448..168309448hg38UCSC Ensembl
chr6:168710128..168710128hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570183
Samples
Known GenesDACT2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062798
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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