A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3549621



Internal ID22418564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95558620..95559959hg38UCSC Ensembl
chr12:95952396..95953735hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg381340
hg191340
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14365649, nssv14365650
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3549621
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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