A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197308



Internal ID22347206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58600166..58600260hg38UCSC Ensembl
chr19:59111533..59111627hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14432480
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3197308
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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