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nsv5396018

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 86 SVs from 20 studies. See in: genome view    
Submitted genomic46,213,101-46,213,152Question Mark
Overlapping variant regions from other studies: 86 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):46,254,592-46,254,643Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5396018Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr346,213,10146,213,152
nsv5396018RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr346,254,59246,254,643

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16933289alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16933289Submitted genomicNC_000003.12:g.462
13101_46213152ins2
80
GRCh38 (hg38)NC_000003.12Chr346,213,10146,213,152
nssv16933289RemappedPerfectNC_000003.11:g.462
54592_46254643ins2
80
GRCh37.p13First PassNC_000003.11Chr346,254,59246,254,643

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)
nssv16933289<0.00116404
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