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nsv5562365

  • 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: 186 SVs from 37 studies. See in: genome view    
Submitted genomic90,357,030-90,357,081Question Mark
Overlapping variant regions from other studies: 186 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):90,900,262-90,900,313Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5562365Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1590,357,03090,357,081
nsv5562365RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1590,900,26290,900,313

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17705119sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17705119Submitted genomicNC_000015.10:g.903
57030_90357081ins7
28
GRCh38 (hg38)NC_000015.10Chr1590,357,03090,357,081
nssv17705119RemappedPerfectNC_000015.9:g.9090
0262_90900313ins72
8
GRCh37.p13First PassNC_000015.9Chr1590,900,26290,900,313

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)
nssv177051190.009566384
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