U.S. flag

An official website of the United States government

nsv5468365

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:338,367

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1457 SVs from 78 studies. See in: genome view    
Submitted genomic126,424,914-126,763,280Question Mark
Overlapping variant regions from other studies: 1457 SVs from 78 studies. See in: genome view    
Remapped(Score: Perfect):125,760,606-126,098,972Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5468365Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5126,424,914126,763,280
nsv5468365RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5125,760,606126,098,972

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16973222duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16973222Submitted genomicNC_000005.10:g.126
424914_126763280du
p
GRCh38 (hg38)NC_000005.10Chr5126,424,914126,763,280
nssv16973222RemappedPerfectNC_000005.9:g.1257
60606_126098972dup
GRCh37.p13First PassNC_000005.9Chr5125,760,606126,098,972

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)
nssv16973222<0.00116404
Support Center