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nsv4570344

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,176

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 23 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):55,680,131-55,682,306Question Mark
Overlapping variant regions from other studies: 23 SVs from 7 studies. See in: genome view    
Submitted genomic56,073,915-56,076,090Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4570344RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1255,680,13155,682,306
nsv4570344Submitted genomicGRCh37.p13Primary AssemblyNC_000012.11Chr1256,073,91556,076,090

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15787772sequence alterationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv15787772RemappedPerfectGRCh38.p12First PassNC_000012.12Chr1255,680,13155,682,306
nssv15787772Submitted genomicGRCh37.p13NC_000012.11Chr1256,073,91556,076,090

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)
nssv157877724.6e-005121694
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