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nsv5473472

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:127

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 147 SVs from 23 studies. See in: genome view    
Submitted genomic110,745,713-110,745,839Question Mark
Overlapping variant regions from other studies: 147 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):110,081,414-110,081,540Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5473472Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5110,745,713110,745,839
nsv5473472RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5110,081,414110,081,540

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16973634deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16973634Submitted genomicNC_000005.10:g.110
745713_110745839de
l
GRCh38 (hg38)NC_000005.10Chr5110,745,713110,745,839
nssv16973634RemappedPerfectNC_000005.9:g.1100
81414_110081540del
GRCh37.p13First PassNC_000005.9Chr5110,081,414110,081,540

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)
nssv16973634<0.00116404
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