A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636168



Internal ID21584473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25140794..25140794hg38UCSC Ensembl
chr10:25429723..25429723hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069717
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636168
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