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nsv5618068

  • 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: 128 SVs from 27 studies. See in: genome view    
Submitted genomic149,380,622-149,380,622Question Mark
Overlapping variant regions from other studies: 128 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):149,098,409-149,098,409Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5618068Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3149,380,622149,380,622
nsv5618068RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3149,098,409149,098,409

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17125411insertionSAMN00006580SequencingSequence alignment9,409

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17125411Submitted genomicNC_000003.12:g.149
380622_149380623in
s98
GRCh38 (hg38)NC_000003.12Chr3149,380,622149,380,622
nssv17125411RemappedPerfectNC_000003.11:g.149
098409_149098410in
s98
GRCh37.p13First PassNC_000003.11Chr3149,098,409149,098,409

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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