A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637398



Internal ID21585703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91066603..91066603hg38UCSC Ensembl
chr8:92078831..92078831hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144160
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637398
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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