A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192928



Internal ID22343444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134138367..134138440hg38UCSC Ensembl
chr11:134008262..134008335hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14443884
SamplesHG00733
Known GenesJAM3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192928
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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