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nsv4573436

  • 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: 44 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):122,484,542-122,484,542Question Mark
Overlapping variant regions from other studies: 44 SVs from 7 studies. See in: genome view    
Submitted genomic125,246,821-125,246,821Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4573436RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr9122,484,542122,484,542
nsv4573436Submitted genomicGRCh37.p13Primary AssemblyNC_000009.11Chr9125,246,821125,246,821

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16086976line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16086976RemappedPerfectNC_000009.12:g.122
484542_122484543in
s1170
GRCh38.p12First PassNC_000009.12Chr9122,484,542122,484,542
nssv16086976Submitted genomicNC_000009.11:g.125
246821_125246822in
s1170
GRCh37.p13NC_000009.11Chr9125,246,821125,246,821

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)
nssv16086976<0.001321692
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