A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14360376



Internal ID22253380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40006933..40009437hg38UCSC Ensembl
chr1:40472605..40475109hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg382505
hg192505
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3244872
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14360376
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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