A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14407319



Internal ID22325232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1626777..1630071hg38UCSC Ensembl
chr19:1626776..1630070hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383295
hg193295
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3199539
Supporting Variants
SamplesNA19240
Known GenesTCF3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14407319
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