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nsv5478494

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:790,894

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 3911 SVs from 118 studies. See in: genome view    
Submitted genomic6,225,437-7,016,330Question Mark
Overlapping variant regions from other studies: 3912 SVs from 118 studies. See in: genome view    
Remapped(Score: Perfect):6,082,958-6,873,852Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5478494Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr86,225,4377,016,330
nsv5478494RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr86,082,9586,873,852

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17008612duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17008612Submitted genomicNC_000008.11:g.622
5437_7016330dup
GRCh38 (hg38)NC_000008.11Chr86,225,4377,016,330
nssv17008612RemappedPerfectNC_000008.10:g.608
2958_6873852dup
GRCh37.p13First PassNC_000008.10Chr86,082,9586,873,852

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)
nssv17008612<0.00116404
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