A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636342



Internal ID21584647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26874085..26874085hg38UCSC Ensembl
chr6:26841864..26841864hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17148903
SamplesHG03732
Known GenesGUSBP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636342
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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