A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637502



Internal ID21585807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67849297..67849297hg38UCSC Ensembl
chr10:69609055..69609055hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071271
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637502
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer