A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580473



Internal ID21528963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168345844..168345938hg38UCSC Ensembl
chr6:168746524..168746618hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159386
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580473
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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