A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14292142



Internal ID22207775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159458825..159525200hg38UCSC Ensembl
chr1:159428615..159494990hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3866376
hg1966376
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3238409
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14292142
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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