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nsv5894692

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:50

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 113 SVs from 26 studies. See in: genome view    
Submitted genomic134,667,273-134,667,322Question Mark
Overlapping variant regions from other studies: 113 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):134,002,963-134,003,012Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5894692Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5134,667,273134,667,322
nsv5894692RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5134,002,963134,003,012

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17417297deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17417297Submitted genomicNC_000005.10:g.134
667273_134667322de
l
GRCh38 (hg38)NC_000005.10Chr5134,667,273134,667,322
nssv17417297RemappedPerfectNC_000005.9:g.1340
02963_134003012del
GRCh37.p13First PassNC_000005.9Chr5134,002,963134,003,012

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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