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nsv5507991

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,803

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 144 SVs from 29 studies. See in: genome view    
Submitted genomic103,182,518-103,185,320Question Mark
Overlapping variant regions from other studies: 144 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):103,648,855-103,651,657Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5507991Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr14103,182,518103,185,320
nsv5507991RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr14103,648,855103,651,657

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17698428deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17698428Submitted genomicNC_000014.9:g.1031
82518_103185320del
GRCh38 (hg38)NC_000014.9Chr14103,182,518103,185,320
nssv17698428RemappedPerfectNC_000014.8:g.1036
48855_103651657del
GRCh37.p13First PassNC_000014.8Chr14103,648,855103,651,657

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)
nssv176984280.002136404
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