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nsv5514202

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,513

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 195 SVs from 28 studies. See in: genome view    
Submitted genomic75,682,821-75,686,333Question Mark
Overlapping variant regions from other studies: 195 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):73,678,901-73,682,413Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5514202Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1775,682,82175,686,333
nsv5514202RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1773,678,90173,682,413

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714649deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714649Submitted genomicNC_000017.11:g.756
82821_75686333del
GRCh38 (hg38)NC_000017.11Chr1775,682,82175,686,333
nssv17714649RemappedPerfectNC_000017.10:g.736
78901_73682413del
GRCh37.p13First PassNC_000017.10Chr1773,678,90173,682,413

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)
nssv17714649<0.00116404
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