A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624728



Internal ID21573033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89266458..89266458hg38UCSC Ensembl
chr8:90278687..90278687hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141433
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624728
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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