A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14420402



Internal ID22157992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1772302..1772366hg38UCSC Ensembl
chr19:1772301..1772365hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3205071
Supporting Variants
SamplesHG00514
Known GenesONECUT3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14420402
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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