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nsv5234296

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,700

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 313 SVs from 62 studies. See in: genome view    
Submitted genomic141,170,201-141,179,900Question Mark
Overlapping variant regions from other studies: 311 SVs from 62 studies. See in: genome view    
Remapped(Score: Perfect):140,549,782-140,559,481Question Mark
Overlapping variant regions from other studies: 152 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):405,377-415,076Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5234296Submitted genomicGRCh38.p13Primary AssemblyNC_000005.10Chr5141,170,201141,179,900
nsv5234296RemappedPerfectGRCh37.p13Primary AssemblySecond PassNC_000005.9Chr5140,549,782140,559,481
nsv5234296RemappedPerfectGRCh37.p13PATCHESFirst PassNW_004775428.1Chr5|NW_00
4775428.1
405,377415,076

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16852760copy number variationSequencingRead depth

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv16852760Submitted genomicGRCh38.p13NC_000005.10Chr5141,170,201141,179,900
nssv16852760RemappedPerfectGRCh37.p13First PassNW_004775428.1Chr5|NW_00
4775428.1
405,377415,076
nssv16852760RemappedPerfectGRCh37.p13Second PassNC_000005.9Chr5140,549,782140,559,481

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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