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nsv5481031

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 205 SVs from 29 studies. See in: genome view    
Submitted genomic150,407,960-150,408,024Question Mark
Overlapping variant regions from other studies: 205 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):150,105,048-150,105,112Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5481031Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7150,407,960150,408,024
nsv5481031RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7150,105,048150,105,112

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17007738deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17007738Submitted genomicNC_000007.14:g.150
407960_150408024de
l
GRCh38 (hg38)NC_000007.14Chr7150,407,960150,408,024
nssv17007738RemappedPerfectNC_000007.13:g.150
105048_150105112de
l
GRCh37.p13First PassNC_000007.13Chr7150,105,048150,105,112

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)
nssv17007738<0.00116404
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