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nsv5903862

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:156

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 125 SVs from 24 studies. See in: genome view    
Submitted genomic171,626,621-171,626,776Question Mark
Overlapping variant regions from other studies: 125 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):171,344,411-171,344,566Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5903862Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3171,626,621171,626,776
nsv5903862RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3171,344,411171,344,566

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17412891deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17412891Submitted genomicNC_000003.12:g.171
626621_171626776de
l
GRCh38 (hg38)NC_000003.12Chr3171,626,621171,626,776
nssv17412891RemappedPerfectNC_000003.11:g.171
344411_171344566de
l
GRCh37.p13First PassNC_000003.11Chr3171,344,411171,344,566

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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