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nsv5485240

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 71 SVs from 16 studies. See in: genome view    
Submitted genomic102,129,166-102,129,223Question Mark
Overlapping variant regions from other studies: 71 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):103,888,923-103,888,980Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5485240Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10102,129,166102,129,223
nsv5485240RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10103,888,923103,888,980

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17683818deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17683818Submitted genomicNC_000010.11:g.102
129166_102129223de
l
GRCh38 (hg38)NC_000010.11Chr10102,129,166102,129,223
nssv17683818RemappedPerfectNC_000010.10:g.103
888923_103888980de
l
GRCh37.p13First PassNC_000010.10Chr10103,888,923103,888,980

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)
nssv17683818<0.00116404
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