U.S. flag

An official website of the United States government

nsv5420949

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 101 SVs from 29 studies. See in: genome view    
Submitted genomic91,848,754-91,848,754Question Mark
Overlapping variant regions from other studies: 101 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):92,242,530-92,242,530Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5420949Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1291,848,75491,848,754
nsv5420949RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1292,242,53092,242,530

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17690019alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17690019Submitted genomicNC_000012.12:g.918
48754_91848755ins3
16
GRCh38 (hg38)NC_000012.12Chr1291,848,75491,848,754
nssv17690019RemappedPerfectNC_000012.11:g.922
42530_92242531ins3
16
GRCh37.p13First PassNC_000012.11Chr1292,242,53092,242,530

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)
nssv176900190.042556380
Support Center