U.S. flag

An official website of the United States government

nsv5503134

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:251

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 87 SVs from 20 studies. See in: genome view    
Submitted genomic30,330,094-30,330,344Question Mark
Overlapping variant regions from other studies: 87 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):30,351,641-30,351,891Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5503134Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1130,330,09430,330,344
nsv5503134RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1130,351,64130,351,891

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17046019deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17046019Submitted genomicNC_000011.10:g.303
30094_30330344del
GRCh38 (hg38)NC_000011.10Chr1130,330,09430,330,344
nssv17046019RemappedPerfectNC_000011.9:g.3035
1641_30351891del
GRCh37.p13First PassNC_000011.9Chr1130,351,64130,351,891

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)
nssv17046019<0.00116404
Support Center