A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219125



Internal ID22364245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131865835..131865970hg38UCSC Ensembl
chr11:131735729..131735864hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1639n152
Supporting Variantsnssv14388449, nssv14446592, nssv14419762
SamplesNA19240, HG00733, HG00514
Known GenesNTM
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219125
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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