A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200229



Internal ID22349711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64759013..64759088hg38UCSC Ensembl
chr11:64526485..64526560hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14442227, nssv14373305, nssv14414417
SamplesNA19240, HG00733, HG00514
Known GenesPYGM
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200229
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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