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nsv5429160

  • 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: 84 SVs from 17 studies. See in: genome view    
Submitted genomic64,989,608-64,989,659Question Mark
Overlapping variant regions from other studies: 84 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):65,456,326-65,456,377Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5429160Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1464,989,60864,989,659
nsv5429160RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1465,456,32665,456,377

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17696756alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17696756Submitted genomicNC_000014.9:g.6498
9608_64989659ins23
7
GRCh38 (hg38)NC_000014.9Chr1464,989,60864,989,659
nssv17696756RemappedPerfectNC_000014.8:g.6545
6326_65456377ins23
7
GRCh37.p13First PassNC_000014.8Chr1465,456,32665,456,377

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)
nssv17696756<0.00116404
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