U.S. flag

An official website of the United States government

nsv5531334

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,737

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 102 SVs from 26 studies. See in: genome view    
Submitted genomic10,265,110-10,272,846Question Mark
Overlapping variant regions from other studies: 102 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):10,245,758-10,253,494Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5531334Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2010,265,11010,272,846
nsv5531334RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2010,245,75810,253,494

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17730821deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17730821Submitted genomicNC_000020.11:g.102
65110_10272846del
GRCh38 (hg38)NC_000020.11Chr2010,265,11010,272,846
nssv17730821RemappedPerfectNC_000020.10:g.102
45758_10253494del
GRCh37.p13First PassNC_000020.10Chr2010,245,75810,253,494

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)
nssv17730821<0.00116404
Support Center