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nsv5488186

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,553

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 229 SVs from 57 studies. See in: genome view    
Submitted genomic104,606,000-104,618,552Question Mark
Overlapping variant regions from other studies: 229 SVs from 57 studies. See in: genome view    
Remapped(Score: Perfect):107,368,281-107,380,833Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5488186Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9104,606,000104,618,552
nsv5488186RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9107,368,281107,380,833

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17027080duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17027080Submitted genomicNC_000009.12:g.104
606000_104618552du
p
GRCh38 (hg38)NC_000009.12Chr9104,606,000104,618,552
nssv17027080RemappedPerfectNC_000009.11:g.107
368281_107380833du
p
GRCh37.p13First PassNC_000009.11Chr9107,368,281107,380,833

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)
nssv17027080<0.00146398
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