A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208783



Internal ID22356972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37545789..37545966hg38UCSC Ensembl
chr19:38036691..38036868hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14448254
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)nsv3208783
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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