A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567161



Internal ID21515493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106535747..106536065hg38UCSC Ensembl
chr6:106983622..106983940hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139923
SamplesHG00731
Known GenesAIM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567161
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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