A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14406167



Internal ID22295287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10703535..10704110hg38UCSC Ensembl
chr19:10814211..10814786hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3225898
Supporting Variants
SamplesNA19240
Known GenesQTRT1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14406167
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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