A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220319



Internal ID22365048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97193181..97193249hg38UCSC Ensembl
chr10:98952938..98953006hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1018n152
Supporting Variantsnssv14379315
SamplesNA19240
Known GenesARHGAP19-SLIT1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220319
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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