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nsv5490505

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,566

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 114 SVs from 28 studies. See in: genome view    
Submitted genomic104,759,903-104,765,468Question Mark
Overlapping variant regions from other studies: 114 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):107,522,184-107,527,749Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5490505Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9104,759,903104,765,468
nsv5490505RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9107,522,184107,527,749

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17026611deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17026611Submitted genomicNC_000009.12:g.104
759903_104765468de
l
GRCh38 (hg38)NC_000009.12Chr9104,759,903104,765,468
nssv17026611RemappedPerfectNC_000009.11:g.107
522184_107527749de
l
GRCh37.p13First PassNC_000009.11Chr9107,522,184107,527,749

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17026611<0.00126404
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