A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3180919



Internal ID22336309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11782764..11782891hg38UCSC Ensembl
chr8:11640273..11640400hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14437803
SamplesHG00514
Known GenesNEIL2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3180919
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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