A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3238409



Internal ID22374145
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14292139, nssv14292142, nssv14292141, nssv14292140, nssv14292146, nssv14292138, nssv14292144, nssv14292143, nssv14292145
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3238409
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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