A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3195966



Internal ID22346062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62143052..62143258hg38UCSC Ensembl
chr11:61910524..61910730hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14391334
SamplesNA19240
Known GenesINCENP
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3195966
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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