A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200857



Internal ID22350247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56703270..56714334hg38UCSC Ensembl
chr11:56470746..56481810hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3811065
hg1911065
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1393n152
Supporting Variantsnssv14375798
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200857
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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