A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584139



Internal ID21532674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166585488..166586677hg38UCSC Ensembl
chr6:166998976..167000165hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381190
hg191190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143894
SamplesNA19238
Known GenesRPS6KA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584139
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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