nsv5499054

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,352

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 248 SVs from 42 studies. See in: genome view    
Submitted genomic33,293,982-33,299,333Question Mark
Overlapping variant regions from other studies: 248 SVs from 42 studies. See in: genome view    
Remapped(Score: Perfect):33,315,528-33,320,879Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5499054Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1133,293,98233,299,333
nsv5499054RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1133,315,52833,320,879

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17044071duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17044071Submitted genomicNC_000011.10:g.332
93982_33299333dup
GRCh38 (hg38)NC_000011.10Chr1133,293,98233,299,333
nssv17044071RemappedPerfectNC_000011.9:g.3331
5528_33320879dup
GRCh37.p13First PassNC_000011.9Chr1133,315,52833,320,879

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)
nssv17044071<0.00146402
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