A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637134



Internal ID21585439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22765795..22765795hg38UCSC Ensembl
chr8:22623308..22623308hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157142
SamplesHG00731
Known GenesPEBP4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637134
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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