A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3187364



Internal ID22339686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107405821..107405875hg38UCSC Ensembl
chr5:106741522..106741576hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14462974
SamplesHG00733
Known GenesEFNA5
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3187364
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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