A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14385810



Internal ID22300160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65216657..65216724hg38UCSC Ensembl
chr11:64984128..64984195hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3210986
Supporting Variants
SamplesNA19240
Known GenesSLC22A20
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14385810
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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