U.S. flag

An official website of the United States government

nsv5546737

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:42

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 148 SVs from 21 studies. See in: genome view    
Submitted genomic125,098,606-125,098,647Question Mark
Overlapping variant regions from other studies: 148 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):126,787,175-126,787,216Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5546737Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10125,098,606125,098,647
nsv5546737RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10126,787,175126,787,216

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17038900insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17038900Submitted genomicNC_000010.11:g.125
098606_125098647in
s59
GRCh38 (hg38)NC_000010.11Chr10125,098,606125,098,647
nssv17038900RemappedPerfectNC_000010.10:g.126
787175_126787216in
s59
GRCh37.p13First PassNC_000010.10Chr10126,787,175126,787,216

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)
nssv170389000.0221376360
Support Center