A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5396892



Internal ID176303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105879990..105880041hg38UCSC Ensembl
chr6:106327865..106327916hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16988653
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5396892
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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