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nsv6270206

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:78

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 163 SVs from 23 studies. See in: genome view    
Submitted genomic128,821,344-128,821,421Question Mark
Overlapping variant regions from other studies: 163 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):131,583,623-131,583,700Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6270206Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9128,821,344128,821,421
nsv6270206RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9131,583,623131,583,700

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17911036deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17911036Submitted genomicNC_000009.12:g.128
821344_128821421de
l
GRCh38 (hg38)NC_000009.12Chr9128,821,344128,821,421
nssv17911036RemappedPerfectNC_000009.11:g.131
583623_131583700de
l
GRCh37.p13First PassNC_000009.11Chr9131,583,623131,583,700

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)
nssv179110360.00132296
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