U.S. flag

An official website of the United States government

nsv5514559

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,849

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 102 SVs from 25 studies. See in: genome view    
Submitted genomic11,336,780-11,340,628Question Mark
Overlapping variant regions from other studies: 102 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):11,447,456-11,451,304Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5514559Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1911,336,78011,340,628
nsv5514559RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1911,447,45611,451,304

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17721399deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17721399Submitted genomicNC_000019.10:g.113
36780_11340628del
GRCh38 (hg38)NC_000019.10Chr1911,336,78011,340,628
nssv17721399RemappedPerfectNC_000019.9:g.1144
7456_11451304del
GRCh37.p13First PassNC_000019.9Chr1911,447,45611,451,304

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)
nssv17721399<0.00116404
Support Center