A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579808



Internal ID21528291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166162673..166162798hg38UCSC Ensembl
chr6:166576161..166576286hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148547
SamplesHG03486
Known GenesT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579808
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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