A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637581



Internal ID21585886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128154256..128154256hg38UCSC Ensembl
chr9:130916535..130916535hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160289
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637581
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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