A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196151



Internal ID22346214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64271021..64271094hg38UCSC Ensembl
chr11:64038493..64038566hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14445443
SamplesHG00733
Known GenesBAD
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196151
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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