A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210632



Internal ID22358468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41140521..41140782hg38UCSC Ensembl
chr19:41646426..41646687hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4273n152
Supporting Variantsnssv14407400
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210632
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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