A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3925435



Internal ID21345506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99675638..99675638hg38UCSC Ensembl
chr7:99273261..99273261hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15203123
SamplesHG002
Known GenesCYP3A5
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3925435
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