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nsv5597488

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:59

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 134 SVs from 28 studies. See in: genome view    
Submitted genomic128,292,646-128,292,704Question Mark
Overlapping variant regions from other studies: 134 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):128,777,191-128,777,249Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5597488Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12128,292,646128,292,704
nsv5597488RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12128,777,191128,777,249

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17078251deletionSAMN00006579SequencingSequence alignment23,265

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17078251Submitted genomicNC_000012.12:g.128
292646_128292704de
lG
GRCh38 (hg38)NC_000012.12Chr12128,292,646128,292,704
nssv17078251RemappedPerfectNC_000012.11:g.128
777191_128777249de
lG
GRCh37.p13First PassNC_000012.11Chr12128,777,191128,777,249

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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