A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192001



Internal ID22342637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60815386..60815563hg38UCSC Ensembl
chr11:60582859..60583036hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14444941, nssv14380198
SamplesNA19240, HG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192001
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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