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nsv5409693

  • 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: 72 SVs from 22 studies. See in: genome view    
Submitted genomic7,007,554-7,007,605Question Mark
Overlapping variant regions from other studies: 72 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):7,028,785-7,028,836Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5409693Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr117,007,5547,007,605
nsv5409693RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr117,028,7857,028,836

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17041746alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17041746Submitted genomicNC_000011.10:g.700
7554_7007605ins280
GRCh38 (hg38)NC_000011.10Chr117,007,5547,007,605
nssv17041746RemappedPerfectNC_000011.9:g.7028
785_7028836ins280
GRCh37.p13First PassNC_000011.9Chr117,028,7857,028,836

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)
nssv17041746<0.00116404
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