A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3939457



Internal ID21359527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127720831..127720831hg38UCSC Ensembl
chr9:130483110..130483110hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15205394
SamplesHG002
Known GenesTTC16
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3939457
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer