A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641475



Internal ID21589780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34904796..34904796hg38UCSC Ensembl
chr9:34904793..34904793hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161641
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641475
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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