A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14292989



Internal ID22256725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168543248..168578925hg38UCSC Ensembl
chr1:168512486..168548163hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3835678
hg1935678
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3236263
Supporting Variants
SamplesNA19238
Known GenesXCL1, XCL2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14292989
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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