A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3230665



Internal ID22371994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131563657..131563811hg38UCSC Ensembl
chr6:131884797..131884951hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14330986, nssv14330991, nssv14330988, nssv14330987, nssv14330990, nssv14330985, nssv14330993, nssv14330989, nssv14330992
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)nsv3230665
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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