U.S. flag

An official website of the United States government

nsv4497965

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 76 SVs from 4 studies. See in: genome view    
Remapped(Score: Perfect):125,816,857-125,816,857Question Mark
Overlapping variant regions from other studies: 76 SVs from 4 studies. See in: genome view    
Submitted genomic127,505,426-127,505,426Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4497965RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr10125,816,857125,816,857
nsv4497965Submitted genomicGRCh37.p13Primary AssemblyNC_000010.10Chr10127,505,426127,505,426

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15994945alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15994945RemappedPerfectNC_000010.11:g.125
816857_125816858in
s281
GRCh38.p12First PassNC_000010.11Chr10125,816,857125,816,857
nssv15994945Submitted genomicNC_000010.10:g.127
505426_127505427in
s281
GRCh37.p13NC_000010.10Chr10127,505,426127,505,426

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)
nssv15994945<0.001421694
Support Center