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nsv5657526

  • 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: 136 SVs from 39 studies. See in: genome view    
Submitted genomic109,209,974-109,209,974Question Mark
Overlapping variant regions from other studies: 136 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):109,647,779-109,647,779Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5657526Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12109,209,974109,209,974
nsv5657526RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12109,647,779109,647,779

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17077393insertionSAMN00001229SequencingSequence alignment1,149

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17077393Submitted genomicNC_000012.12:g.109
209974_109209975in
s177
GRCh38 (hg38)NC_000012.12Chr12109,209,974109,209,974
nssv17077393RemappedPerfectNC_000012.11:g.109
647779_109647780in
s177
GRCh37.p13First PassNC_000012.11Chr12109,647,779109,647,779

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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