A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14301012



Internal ID22299670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58097022..58097277hg38UCSC Ensembl
chr20:56672078..56672333hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3558306
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14301012
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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