A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3945970



Internal ID21366039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13424322..13424322hg38UCSC Ensembl
chr9:13424321..13424321hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg381416
hg191416
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204779
SamplesHG002
Known GenesFLJ41200
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3945970
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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