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nsv5233838

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,000

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 287 SVs from 61 studies. See in: genome view    
Submitted genomic141,179,801-141,188,800Question Mark
Overlapping variant regions from other studies: 285 SVs from 61 studies. See in: genome view    
Remapped(Score: Good):140,559,382-140,568,373Question Mark
Overlapping variant regions from other studies: 109 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):414,977-423,976Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5233838Submitted genomicGRCh38.p13Primary AssemblyNC_000005.10Chr5141,179,801141,188,800
nsv5233838RemappedGoodGRCh37.p13Primary AssemblySecond PassNC_000005.9Chr5140,559,382140,568,373
nsv5233838RemappedPerfectGRCh37.p13PATCHESFirst PassNW_004775428.1Chr5|NW_00
4775428.1
414,977423,976

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16848362copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16848362Submitted genomicGRCh38.p13NC_000005.10Chr5141,179,801141,188,800
nssv16848362RemappedPerfectGRCh37.p13First PassNW_004775428.1Chr5|NW_00
4775428.1
414,977423,976
nssv16848362RemappedGoodGRCh37.p13Second PassNC_000005.9Chr5140,559,382140,568,373

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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