U.S. flag

An official website of the United States government

nsv5514313

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:51

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 70 SVs from 22 studies. See in: genome view    
Submitted genomic19,583,020-19,583,070Question Mark
Overlapping variant regions from other studies: 70 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):19,594,342-19,594,392Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5514313Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1619,583,02019,583,070
nsv5514313RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1619,594,34219,594,392

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17706141deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17706141Submitted genomicNC_000016.10:g.195
83020_19583070del
GRCh38 (hg38)NC_000016.10Chr1619,583,02019,583,070
nssv17706141RemappedPerfectNC_000016.9:g.1959
4342_19594392del
GRCh37.p13First PassNC_000016.9Chr1619,594,34219,594,392

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)
nssv17706141<0.00116404
Support Center