A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200956



Internal ID22350334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118947982..118948124hg38UCSC Ensembl
chr11:118818692..118818834hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14443431
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)nsv3200956
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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