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nsv5489273

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:87,590

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 437 SVs from 63 studies. See in: genome view    
Submitted genomic90,836,021-90,923,610Question Mark
Overlapping variant regions from other studies: 437 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):93,598,303-93,685,892Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5489273Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr990,836,02190,923,610
nsv5489273RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr993,598,30393,685,892

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17024026duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17024026Submitted genomicNC_000009.12:g.908
36021_90923610dup
GRCh38 (hg38)NC_000009.12Chr990,836,02190,923,610
nssv17024026RemappedPerfectNC_000009.11:g.935
98303_93685892dup
GRCh37.p13First PassNC_000009.11Chr993,598,30393,685,892

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)
nssv17024026<0.00126404
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