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nsv5480275

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,282

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 115 SVs from 36 studies. See in: genome view    
Submitted genomic56,088,566-56,089,847Question Mark
Overlapping variant regions from other studies: 115 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):56,156,259-56,157,540Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5480275Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr756,088,56656,089,847
nsv5480275RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr756,156,25956,157,540

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16996432deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16996432Submitted genomicNC_000007.14:g.560
88566_56089847del
GRCh38 (hg38)NC_000007.14Chr756,088,56656,089,847
nssv16996432RemappedPerfectNC_000007.13:g.561
56259_56157540del
GRCh37.p13First PassNC_000007.13Chr756,156,25956,157,540

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)
nssv16996432<0.00116404
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