A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199289



Internal ID22348894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28674051..28674221hg38UCSC Ensembl
chr10:28962980..28963150hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14440232
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)nsv3199289
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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