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nsv5914132

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,780,669

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 24174 SVs from 128 studies. See in: genome view    
Submitted genomic26,936,027-36,716,695Question Mark
Overlapping variant regions from other studies: 24175 SVs from 128 studies. See in: genome view    
Remapped(Score: Perfect):26,975,646-36,756,300Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5914132Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr726,936,02736,716,695
nsv5914132RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr726,975,64636,756,300

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17431581deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17431581Submitted genomicNC_000007.14:g.269
36027_36716695del
GRCh38 (hg38)NC_000007.14Chr726,936,02736,716,695
nssv17431581RemappedPerfectNC_000007.13:g.269
75646_36756300del
GRCh37.p13First PassNC_000007.13Chr726,975,64636,756,300

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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