A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951418



Internal ID21371487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61877438..61877438hg38UCSC Ensembl
chr15:62169637..62169637hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15195273
SamplesHG002
Known GenesVPS13C
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951418
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