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nsv5440172

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,765

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 98 SVs from 29 studies. See in: genome view    
Submitted genomic101,562,004-101,564,768Question Mark
Overlapping variant regions from other studies: 98 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):101,280,848-101,283,612Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5440172Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3101,562,004101,564,768
nsv5440172RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3101,280,848101,283,612

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17734909deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17734909Submitted genomicNC_000003.12:g.101
562004_101564768de
l
GRCh38 (hg38)NC_000003.12Chr3101,562,004101,564,768
nssv17734909RemappedPerfectNC_000003.11:g.101
280848_101283612de
l
GRCh37.p13First PassNC_000003.11Chr3101,280,848101,283,612

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)
nssv17734909<0.00146404
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