A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3242669



Internal ID22375342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57521695..57526505hg38UCSC Ensembl
chr19:58033063..58037873hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg384811
hg194811
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14287471, nssv14287470
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3242669
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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