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nsv5913209

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:148

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 162 SVs from 47 studies. See in: genome view    
Submitted genomic90,841,972-90,842,119Question Mark
Overlapping variant regions from other studies: 162 SVs from 47 studies. See in: genome view    
Remapped(Score: Perfect):93,604,254-93,604,401Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5913209Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr990,841,97290,842,119
nsv5913209RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr993,604,25493,604,401

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17439889deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17439889Submitted genomicNC_000009.12:g.908
41972_90842119del
GRCh38 (hg38)NC_000009.12Chr990,841,97290,842,119
nssv17439889RemappedPerfectNC_000009.11:g.936
04254_93604401del
GRCh37.p13First PassNC_000009.11Chr993,604,25493,604,401

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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