A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109311



Internal ID22018544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31724302..31724302hg38UCSC Ensembl
chr21:33096615..33096615hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645709
Samples
Known GenesSCAF4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109311
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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