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nsv5395690

  • 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: 82 SVs from 19 studies. See in: genome view    
Submitted genomic40,769,116-40,769,167Question Mark
Overlapping variant regions from other studies: 82 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):40,769,218-40,769,269Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5395690Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr540,769,11640,769,167
nsv5395690RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr540,769,21840,769,269

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16964493alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16964493Submitted genomicNC_000005.10:g.407
69116_40769167ins2
79
GRCh38 (hg38)NC_000005.10Chr540,769,11640,769,167
nssv16964493RemappedPerfectNC_000005.9:g.4076
9218_40769269ins27
9
GRCh37.p13First PassNC_000005.9Chr540,769,21840,769,269

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)
nssv16964493<0.00116404
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