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nsv5474442

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:283

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 146 SVs from 55 studies. See in: genome view    
Submitted genomic113,174,817-113,175,099Question Mark
Overlapping variant regions from other studies: 146 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):115,937,097-115,937,379Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5474442Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9113,174,817113,175,099
nsv5474442RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9115,937,097115,937,379

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17026366deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17026366Submitted genomicNC_000009.12:g.113
174817_113175099de
l
GRCh38 (hg38)NC_000009.12Chr9113,174,817113,175,099
nssv17026366RemappedPerfectNC_000009.11:g.115
937097_115937379de
l
GRCh37.p13First PassNC_000009.11Chr9115,937,097115,937,379

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)
nssv170263660.82552816404
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