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nsv5495562

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,085

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 125 SVs from 24 studies. See in: genome view    
Submitted genomic121,954,605-121,957,689Question Mark
Overlapping variant regions from other studies: 125 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):123,714,120-123,717,204Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5495562Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10121,954,605121,957,689
nsv5495562RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10123,714,120123,717,204

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17040368deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17040368Submitted genomicNC_000010.11:g.121
954605_121957689de
l
GRCh38 (hg38)NC_000010.11Chr10121,954,605121,957,689
nssv17040368RemappedPerfectNC_000010.10:g.123
714120_123717204de
l
GRCh37.p13First PassNC_000010.10Chr10123,714,120123,717,204

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)
nssv17040368<0.00116404
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