U.S. flag

An official website of the United States government

nsv4510218

  • 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: 33 SVs from 9 studies. See in: genome view    
Remapped(Score: Perfect):14,037,785-14,037,785Question Mark
Overlapping variant regions from other studies: 33 SVs from 9 studies. See in: genome view    
Submitted genomic13,941,102-13,941,102Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4510218RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1714,037,78514,037,785
nsv4510218Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1713,941,10213,941,102

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16017644alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16017644RemappedPerfectNC_000017.11:g.140
37785_14037786ins2
81
GRCh38.p12First PassNC_000017.11Chr1714,037,78514,037,785
nssv16017644Submitted genomicNC_000017.10:g.139
41102_13941103ins2
81
GRCh37.p13NC_000017.10Chr1713,941,10213,941,102

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)
nssv160176444.6e-005121694
Support Center