A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628725



Internal ID21577030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27777601..27777601hg38UCSC Ensembl
chr10:28066530..28066530hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069590
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628725
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