A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625918



Internal ID21574223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14459727..14459727hg38UCSC Ensembl
chr9:14459725..14459725hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161015
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625918
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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