A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3248494



Internal ID22377004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13835204..13865076hg38UCSC Ensembl
chr6:13835435..13865307hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3829873
hg1929873
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14327496, nssv14327495, nssv14327494
SamplesHG00732, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3248494
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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