A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3187431



Internal ID22339722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25881945..25882261hg38UCSC Ensembl
chr6:25882173..25882489hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14461612
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3187431
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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