A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635576



Internal ID21583881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100019622..100019622hg38UCSC Ensembl
chr9:102781904..102781904hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147431
SamplesNA19238
Known GenesERP44
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635576
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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