A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074428



Internal ID21983661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27485647..27485647hg38UCSC Ensembl
chr6:27453426..27453426hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576046
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074428
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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