nsv5578434

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:72

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 129 SVs from 42 studies. See in: genome view    
Submitted genomic52,444,714-52,444,785Question Mark
Overlapping variant regions from other studies: 129 SVs from 42 studies. See in: genome view    
Remapped(Score: Perfect):52,478,730-52,478,801Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5578434Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr352,444,71452,444,785
nsv5578434RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr352,478,73052,478,801

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17130897deletionSAMN00006579SequencingSequence alignment23,265

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17130897Submitted genomicNC_000003.12:g.524
44714_52444785delC
GRCh38 (hg38)NC_000003.12Chr352,444,71452,444,785
nssv17130897RemappedPerfectNC_000003.11:g.524
78730_52478801delC
GRCh37.p13First PassNC_000003.11Chr352,478,73052,478,801

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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