A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5397737



Internal ID177141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28908301..28908352hg38UCSC Ensembl
chr6:28876078..28876129hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16980911
Samples
Known GenesTRIM27
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5397737
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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