A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667770



Internal ID21616075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45428105..45428105hg38UCSC Ensembl
chr21:46848020..46848020hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38995
hg19995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124865
SamplesHG03065
Known GenesCOL18A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667770
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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