A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069037



Internal ID21978270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27230430..27230430hg38UCSC Ensembl
chr6:27198209..27198209hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577421
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069037
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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