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nsv5417000

  • 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: 162 SVs from 20 studies. See in: genome view    
Submitted genomic28,071,707-28,071,758Question Mark
Overlapping variant regions from other studies: 162 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):25,651,671-25,651,722Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5417000Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1828,071,70728,071,758
nsv5417000RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1825,651,67125,651,722

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17716873alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17716873Submitted genomicNC_000018.10:g.280
71707_28071758ins2
81
GRCh38 (hg38)NC_000018.10Chr1828,071,70728,071,758
nssv17716873RemappedPerfectNC_000018.9:g.2565
1671_25651722ins28
1
GRCh37.p13First PassNC_000018.9Chr1825,651,67125,651,722

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)
nssv17716873<0.00116404
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