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nsv5487425

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,748

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 495 SVs from 55 studies. See in: genome view    
Submitted genomic17,879,545-17,896,292Question Mark
Overlapping variant regions from other studies: 495 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):17,737,054-17,753,801Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5487425Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr817,879,54517,896,292
nsv5487425RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr817,737,05417,753,801

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17007548deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17007548Submitted genomicNC_000008.11:g.178
79545_17896292del
GRCh38 (hg38)NC_000008.11Chr817,879,54517,896,292
nssv17007548RemappedPerfectNC_000008.10:g.177
37054_17753801del
GRCh37.p13First PassNC_000008.10Chr817,737,05417,753,801

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)
nssv17007548<0.00116404
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