A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17147431



Internal ID21495765
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 StatusS
Merged Variantsnsv5635576
Supporting Variants
SamplesNA19238
Known GenesERP44
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17147431
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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