A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14289821



Internal ID22231559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60132130..60145283hg38UCSC Ensembl
chr2:60359265..60372418hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3813154
hg1913154
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3242848
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14289821
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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