A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17143253



Internal ID21499784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109499103..109499103hg38UCSC Ensembl
chr9:112261383..112261383hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643548
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17143253
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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