A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3928449



Internal ID21348518
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 StatusM
Merged Variants
Supporting Variantsnssv15205118
SamplesHG002
Known GenesADAMTSL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3928449
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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