A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14316575



Internal ID22325500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87807402..87807402hg38UCSC Ensembl
chr4:88728554..88728554hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3563611
Supporting Variants
SamplesNA19240
Known GenesIBSP
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14316575
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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