U.S. flag

An official website of the United States government

nsv5398356

  • 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: 204 SVs from 38 studies. See in: genome view    
Submitted genomic31,502,943-31,502,994Question Mark
Overlapping variant regions from other studies: 204 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):31,470,720-31,470,771Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5398356Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr631,502,94331,502,994
nsv5398356RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr631,470,72031,470,771

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16980417alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16980417Submitted genomicNC_000006.12:g.315
02943_31502994ins2
80
GRCh38 (hg38)NC_000006.12Chr631,502,94331,502,994
nssv16980417RemappedPerfectNC_000006.11:g.314
70720_31470771ins2
80
GRCh37.p13First PassNC_000006.11Chr631,470,72031,470,771

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)
nssv16980417<0.00116404
Support Center