A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3242781



Internal ID22375380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22411628..22415968hg38UCSC Ensembl
chr20:22392266..22396606hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg384341
hg194341
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14297660
SamplesHG00514
Known GenesLOC284788
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3242781
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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