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nsv4256840

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:257

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 24 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):40,126,632-40,126,888Question Mark
Overlapping variant regions from other studies: 22 SVs from 7 studies. See in: genome view    
Submitted genomic38,282,885-38,283,141Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4256840RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1740,126,63240,126,888
nsv4256840Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1738,282,88538,283,141

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15836283deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15836283RemappedPerfectNC_000017.11:g.401
26632_40126888del
GRCh38.p12First PassNC_000017.11Chr1740,126,63240,126,888
nssv15836283Submitted genomicNC_000017.10:g.382
82885_38283141del
GRCh37.p13NC_000017.10Chr1738,282,88538,283,141

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)
nssv158362834.6e-005121694
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