A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634777



Internal ID21583082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109804456..109804456hg38UCSC Ensembl
chr8:110816685..110816685hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17152340
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634777
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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