U.S. flag

An official website of the United States government

nsv5560879

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 167 SVs from 18 studies. See in: genome view    
Submitted genomic35,687,358-35,687,409Question Mark
Overlapping variant regions from other studies: 167 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):33,267,322-33,267,373Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5560879Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1835,687,35835,687,409
nsv5560879RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1833,267,32233,267,373

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17717323line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17717323Submitted genomicNC_000018.10:g.356
87358_35687409ins4
55
GRCh38 (hg38)NC_000018.10Chr1835,687,35835,687,409
nssv17717323RemappedPerfectNC_000018.9:g.3326
7322_33267373ins45
5
GRCh37.p13First PassNC_000018.9Chr1833,267,32233,267,373

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)
nssv17717323<0.00116404
Support Center