A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14460190



Internal ID22245651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33858767..33858907hg38UCSC Ensembl
chr19:34349672..34349812hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223148
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14460190
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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