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nsv5487358

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,118

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 135 SVs from 34 studies. See in: genome view    
Submitted genomic75,128,773-75,135,890Question Mark
Overlapping variant regions from other studies: 135 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):76,888,531-76,895,648Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5487358Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1075,128,77375,135,890
nsv5487358RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1076,888,53176,895,648

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17683785deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17683785Submitted genomicNC_000010.11:g.751
28773_75135890del
GRCh38 (hg38)NC_000010.11Chr1075,128,77375,135,890
nssv17683785RemappedPerfectNC_000010.10:g.768
88531_76895648del
GRCh37.p13First PassNC_000010.10Chr1076,888,53176,895,648

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)
nssv17683785<0.00126404
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