A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3242087



Internal ID22375164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16225003..16225064hg38UCSC Ensembl
chr2:16406271..16406332hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14288297, nssv14288296, nssv14288298
SamplesHG00731, HG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3242087
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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