A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455526



Internal ID233605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106321580..106323131hg38UCSC Ensembl
chr6:106769455..106771006hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381552
hg191552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986664
Samples
Known GenesATG5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455526
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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