A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199646



Internal ID22349204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1009328..1009383hg38UCSC Ensembl
chr10:1055268..1055323hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14385651
SamplesNA19240
Known GenesGTPBP4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199646
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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