A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626860



Internal ID21575165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6404930..6404930hg38UCSC Ensembl
chr10:6446892..6446892hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071220
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626860
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