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nsv5870961

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:858

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 157 SVs from 23 studies. See in: genome view    
Submitted genomic103,108,453-103,109,310Question Mark
Overlapping variant regions from other studies: 157 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):103,574,009-103,574,866Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5870961Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1103,108,453103,109,310
nsv5870961RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1103,574,009103,574,866

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17367773deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17367773Submitted genomicNC_000001.11:g.103
108453_103109310de
l
GRCh38 (hg38)NC_000001.11Chr1103,108,453103,109,310
nssv17367773RemappedPerfectNC_000001.10:g.103
574009_103574866de
l
GRCh37.p13First PassNC_000001.10Chr1103,574,009103,574,866

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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