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nsv5503395

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,884

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 169 SVs from 27 studies. See in: genome view    
Submitted genomic125,031,186-125,037,069Question Mark
Overlapping variant regions from other studies: 169 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):126,719,755-126,725,638Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5503395Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10125,031,186125,037,069
nsv5503395RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10126,719,755126,725,638

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17038898deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17038898Submitted genomicNC_000010.11:g.125
031186_125037069de
l
GRCh38 (hg38)NC_000010.11Chr10125,031,186125,037,069
nssv17038898RemappedPerfectNC_000010.10:g.126
719755_126725638de
l
GRCh37.p13First PassNC_000010.10Chr10126,719,755126,725,638

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)
nssv17038898<0.00116404
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