A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069821



Internal ID21979054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19940186..19940186hg38UCSC Ensembl
chr6:19940417..19940417hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559305
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069821
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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