A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5408903



Internal ID188226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105192901..105192952hg38UCSC Ensembl
chr6:105640776..105640827hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16988613
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5408903
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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