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nsv4550461

  • 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: 29 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):170,482,067-170,482,067Question Mark
Overlapping variant regions from other studies: 29 SVs from 5 studies. See in: genome view    
Submitted genomic170,199,856-170,199,856Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4550461RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3170,482,067170,482,067
nsv4550461Submitted genomicGRCh37.p13Primary AssemblyNC_000003.11Chr3170,199,856170,199,856

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16050670insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16050670RemappedPerfectNC_000003.12:g.170
482067_170482068in
s72
GRCh38.p12First PassNC_000003.12Chr3170,482,067170,482,067
nssv16050670Submitted genomicNC_000003.11:g.170
199856_170199857in
s72
GRCh37.p13NC_000003.11Chr3170,199,856170,199,856

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)
nssv16050670<0.001521694
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