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nsv5428504

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:60

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 179 SVs from 25 studies. See in: genome view    
Submitted genomic93,306,663-93,306,722Question Mark
Overlapping variant regions from other studies: 179 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):93,958,916-93,958,975Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5428504Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1393,306,66393,306,722
nsv5428504RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1393,958,91693,958,975

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17691181alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17691181Submitted genomicNC_000013.11:g.933
06663_93306722ins2
81
GRCh38 (hg38)NC_000013.11Chr1393,306,66393,306,722
nssv17691181RemappedPerfectNC_000013.10:g.939
58916_93958975ins2
81
GRCh37.p13First PassNC_000013.10Chr1393,958,91693,958,975

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17691181<0.00166404
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