A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560664



Internal ID22429460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61762420..61762420hg38UCSC Ensembl
chr14:62229138..62229138hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14370245, nssv14370246
SamplesNA19239, HG00514
Known GenesSNAPC1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560664
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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