A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14393513



Internal ID22286399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34537752..34540826hg38UCSC Ensembl
chr19:35028657..35031731hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg383075
hg193075
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3198525
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14393513
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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