A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159985



Internal ID21510454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133539653..133539653hg38UCSC Ensembl
chr9:136404775..136404775hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634619
Supporting Variants
SamplesNA24385
Known GenesADAMTSL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159985
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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