A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14393776



Internal ID22310257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13675093..13675093hg38UCSC Ensembl
chr18:13675092..13675092hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3550763
Supporting Variants
SamplesNA19240
Known GenesFAM210A
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14393776
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