A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633937



Internal ID21582242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42381073..42381073hg38UCSC Ensembl
chr8:42238591..42238591hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158924
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633937
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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