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nsv5506225

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:101

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 96 SVs from 29 studies. See in: genome view    
Submitted genomic106,442,674-106,442,774Question Mark
Overlapping variant regions from other studies: 96 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):106,836,452-106,836,552Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5506225Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12106,442,674106,442,774
nsv5506225RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12106,836,452106,836,552

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17690620deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17690620Submitted genomicNC_000012.12:g.106
442674_106442774de
l
GRCh38 (hg38)NC_000012.12Chr12106,442,674106,442,774
nssv17690620RemappedPerfectNC_000012.11:g.106
836452_106836552de
l
GRCh37.p13First PassNC_000012.11Chr12106,836,452106,836,552

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)
nssv176906200.006396404
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