A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3932350



Internal ID21352419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10792054..10792054hg38UCSC Ensembl
chr10:10834017..10834017hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381028
hg191028
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191522
SamplesHG002
Known GenesSFTA1P
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3932350
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