A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202525



Internal ID22351679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79087937..79088547hg38UCSC Ensembl
chr14:79554280..79554890hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38611
hg19611
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14404484
SamplesNA19240
Known GenesNRXN3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202525
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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