A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159613



Internal ID21451973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111600860..111600860hg38UCSC Ensembl
chr9:114363140..114363140hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381499
hg191499
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640749
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159613
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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