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nsv5457167

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:58,853

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 308 SVs from 61 studies. See in: genome view    
Submitted genomic30,726,973-30,785,825Question Mark
Overlapping variant regions from other studies: 308 SVs from 61 studies. See in: genome view    
Remapped(Score: Perfect):30,694,750-30,753,602Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5457167Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr630,726,97330,785,825
nsv5457167RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr630,694,75030,753,602

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17735509duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17735509Submitted genomicNC_000006.12:g.307
26973_30785825dup
GRCh38 (hg38)NC_000006.12Chr630,726,97330,785,825
nssv17735509RemappedPerfectNC_000006.11:g.306
94750_30753602dup
GRCh37.p13First PassNC_000006.11Chr630,694,75030,753,602

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)
nssv17735509<0.00136404
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