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nsv5922254

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:221

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 151 SVs from 46 studies. See in: genome view    
Submitted genomic7,751,854-7,752,074Question Mark
Overlapping variant regions from other studies: 151 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):7,793,817-7,794,037Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5922254Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr107,751,8547,752,074
nsv5922254RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr107,793,8177,794,037

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17364395deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17364395Submitted genomicNC_000010.11:g.775
1854_7752074del
GRCh38 (hg38)NC_000010.11Chr107,751,8547,752,074
nssv17364395RemappedPerfectNC_000010.10:g.779
3817_7794037del
GRCh37.p13First PassNC_000010.10Chr107,793,8177,794,037

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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