U.S. flag

An official website of the United States government

nsv5532090

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,722

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 124 SVs from 28 studies. See in: genome view    
Submitted genomic67,223,660-67,225,381Question Mark
Overlapping variant regions from other studies: 124 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):67,257,563-67,259,284Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5532090Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1667,223,66067,225,381
nsv5532090RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1667,257,56367,259,284

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17707488deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17707488Submitted genomicNC_000016.10:g.672
23660_67225381del
GRCh38 (hg38)NC_000016.10Chr1667,223,66067,225,381
nssv17707488RemappedPerfectNC_000016.9:g.6725
7563_67259284del
GRCh37.p13First PassNC_000016.9Chr1667,257,56367,259,284

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)
nssv17707488<0.00136404
Support Center