A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061553



Internal ID21970786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56683394..56683394hg38UCSC Ensembl
chr6:56548192..56548192hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566215
Samples
Known GenesDST, RNU6-71P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061553
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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