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nsv5507095

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 87 SVs from 15 studies. See in: genome view    
Submitted genomic118,358,530-118,358,600Question Mark
Overlapping variant regions from other studies: 87 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):120,118,042-120,118,112Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5507095Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10118,358,530118,358,600
nsv5507095RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10120,118,042120,118,112

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17040797deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17040797Submitted genomicNC_000010.11:g.118
358530_118358600de
l
GRCh38 (hg38)NC_000010.11Chr10118,358,530118,358,600
nssv17040797RemappedPerfectNC_000010.10:g.120
118042_120118112de
l
GRCh37.p13First PassNC_000010.10Chr10120,118,042120,118,112

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)
nssv17040797<0.00116404
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