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nsv5397602

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 112 SVs from 21 studies. See in: genome view    
Submitted genomic40,247,696-40,247,705Question Mark
Overlapping variant regions from other studies: 112 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):40,713,368-40,713,377Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5397602Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr140,247,69640,247,705
nsv5397602RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr140,713,36840,713,377

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16901532alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16901532Submitted genomicNC_000001.11:g.402
47696_40247705ins2
81
GRCh38 (hg38)NC_000001.11Chr140,247,69640,247,705
nssv16901532RemappedPerfectNC_000001.10:g.407
13368_40713377ins2
81
GRCh37.p13First PassNC_000001.10Chr140,713,36840,713,377

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)
nssv16901532<0.00116404
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