U.S. flag

An official website of the United States government

nsv5633834

  • 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: 188 SVs from 29 studies. See in: genome view    
Submitted genomic86,791,687-86,791,687Question Mark
Overlapping variant regions from other studies: 188 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):88,551,444-88,551,444Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5633834Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1086,791,68786,791,687
nsv5633834RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1088,551,44488,551,444

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17071358insertionSAMN00001695SequencingSequence alignment6,153

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17071358Submitted genomicNC_000010.11:g.867
91687_86791688ins5
7
GRCh38 (hg38)NC_000010.11Chr1086,791,68786,791,687
nssv17071358RemappedPerfectNC_000010.10:g.885
51444_88551445ins5
7
GRCh37.p13First PassNC_000010.10Chr1088,551,44488,551,444

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.

Support Center