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nsv5406954

  • 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: 137 SVs from 20 studies. See in: genome view    
Submitted genomic17,768,241-17,768,292Question Mark
Overlapping variant regions from other studies: 137 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):17,769,864-17,769,915Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5406954Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr417,768,24117,768,292
nsv5406954RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr417,769,86417,769,915

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16948313alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16948313Submitted genomicNC_000004.12:g.177
68241_17768292ins2
79
GRCh38 (hg38)NC_000004.12Chr417,768,24117,768,292
nssv16948313RemappedPerfectNC_000004.11:g.177
69864_17769915ins2
79
GRCh37.p13First PassNC_000004.11Chr417,769,86417,769,915

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)
nssv16948313<0.00116404
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