A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642306



Internal ID21590611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4183709..4183709hg38UCSC Ensembl
chr10:4225901..4225901hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070417
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642306
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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