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nsv5517394

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,523

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 177 SVs from 36 studies. See in: genome view    
Submitted genomic75,488,773-75,490,295Question Mark
Overlapping variant regions from other studies: 177 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):75,522,671-75,524,193Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5517394Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1675,488,77375,490,295
nsv5517394RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1675,522,67175,524,193

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17710187deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17710187Submitted genomicNC_000016.10:g.754
88773_75490295del
GRCh38 (hg38)NC_000016.10Chr1675,488,77375,490,295
nssv17710187RemappedPerfectNC_000016.9:g.7552
2671_75524193del
GRCh37.p13First PassNC_000016.9Chr1675,522,67175,524,193

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)
nssv177101870.002166404
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