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nsv4573466

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 40 SVs from 4 studies. See in: genome view    
Remapped(Score: Perfect):28,433,799-28,433,799Question Mark
Overlapping variant regions from other studies: 40 SVs from 4 studies. See in: genome view    
Submitted genomic29,007,936-29,007,936Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4573466RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1328,433,79928,433,799
nsv4573466Submitted genomicGRCh37.p13Primary AssemblyNC_000013.10Chr1329,007,93629,007,936

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16004415line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16004415RemappedPerfectNC_000013.11:g.284
33799_28433800ins7
32
GRCh38.p12First PassNC_000013.11Chr1328,433,79928,433,799
nssv16004415Submitted genomicNC_000013.10:g.290
07936_29007937ins7
32
GRCh37.p13NC_000013.10Chr1329,007,93629,007,936

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)
nssv160044154.6e-005121694
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