A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578397



Internal ID21526864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101623358..101623520hg38UCSC Ensembl
chr8:102635586..102635748hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17154537
SamplesNA19238
Known GenesGRHL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578397
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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