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nsv4269221

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19,629

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 41 SVs from 8 studies. See in: genome view    
Remapped(Score: Perfect):36,005,948-36,025,576Question Mark
Overlapping variant regions from other studies: 41 SVs from 8 studies. See in: genome view    
Submitted genomic36,496,850-36,516,478Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4269221RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000019.10Chr1936,005,94836,025,576
nsv4269221Submitted genomicGRCh37.p13Primary AssemblyNC_000019.9Chr1936,496,85036,516,478

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15961612duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15961612RemappedPerfectNC_000019.10:g.360
05948_36025576dup
GRCh38.p12First PassNC_000019.10Chr1936,005,94836,025,576
nssv15961612Submitted genomicNC_000019.9:g.3649
6850_36516478dup
GRCh37.p13NC_000019.9Chr1936,496,85036,516,478

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)
nssv159616129.2e-005221694
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