U.S. flag

An official website of the United States government

nsv5495898

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,451

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 307 SVs from 63 studies. See in: genome view    
Submitted genomic10,408,650-10,422,100Question Mark
Overlapping variant regions from other studies: 308 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):10,561,249-10,574,699Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5495898Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1210,408,65010,422,100
nsv5495898RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1210,561,24910,574,699

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17053030duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17053030Submitted genomicNC_000012.12:g.104
08650_10422100dup
GRCh38 (hg38)NC_000012.12Chr1210,408,65010,422,100
nssv17053030RemappedPerfectNC_000012.11:g.105
61249_10574699dup
GRCh37.p13First PassNC_000012.11Chr1210,561,24910,574,699

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)
nssv17053030<0.00136400
Support Center