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nsv5658541

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 171 SVs from 28 studies. See in: genome view    
Submitted genomic92,631,082-92,631,082Question Mark
Overlapping variant regions from other studies: 171 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):93,174,312-93,174,312Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5658541Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1592,631,08292,631,082
nsv5658541RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1593,174,31293,174,312

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17095119insertionSAMN00006466SequencingSequence alignment4,625

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17095119Submitted genomicNC_000015.10:g.926
31082_92631083ins1
39
GRCh38 (hg38)NC_000015.10Chr1592,631,08292,631,082
nssv17095119RemappedPerfectNC_000015.9:g.9317
4312_93174313ins13
9
GRCh37.p13First PassNC_000015.9Chr1593,174,31293,174,312

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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