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nsv6151507

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:307

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 115 SVs from 42 studies. See in: genome view    
Submitted genomic85,099,847-85,100,153Question Mark
Overlapping variant regions from other studies: 115 SVs from 42 studies. See in: genome view    
Remapped(Score: Perfect):85,326,970-85,327,276Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6151507Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr285,099,84785,100,153
nsv6151507RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr285,326,97085,327,276

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17864910deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17864910Submitted genomicNC_000002.12:g.850
99847_85100153del
GRCh38 (hg38)NC_000002.12Chr285,099,84785,100,153
nssv17864910RemappedPerfectNC_000002.11:g.853
26970_85327276del
GRCh37.p13First PassNC_000002.11Chr285,326,97085,327,276

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)
nssv17864910<0.00122086
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