U.S. flag

An official website of the United States government

nsv5500949

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,183

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 92 SVs from 25 studies. See in: genome view    
Submitted genomic98,613,548-98,614,730Question Mark
Overlapping variant regions from other studies: 92 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):99,007,326-99,008,508Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5500949Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1298,613,54898,614,730
nsv5500949RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1299,007,32699,008,508

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17690220deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17690220Submitted genomicNC_000012.12:g.986
13548_98614730del
GRCh38 (hg38)NC_000012.12Chr1298,613,54898,614,730
nssv17690220RemappedPerfectNC_000012.11:g.990
07326_99008508del
GRCh37.p13First PassNC_000012.11Chr1299,007,32699,008,508

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)
nssv17690220<0.00116404
Support Center