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nsv4224114

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:74

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 18 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):110,033,125-110,033,198Question Mark
Overlapping variant regions from other studies: 18 SVs from 5 studies. See in: genome view    
Submitted genomic110,470,930-110,471,003Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4224114RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr12110,033,125110,033,198
nsv4224114Submitted genomicGRCh37.p13Primary AssemblyNC_000012.11Chr12110,470,930110,471,003

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15813478deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15813478RemappedPerfectNC_000012.12:g.110
033125_110033198de
l
GRCh38.p12First PassNC_000012.12Chr12110,033,125110,033,198
nssv15813478Submitted genomicNC_000012.11:g.110
470930_110471003de
l
GRCh37.p13NC_000012.11Chr12110,470,930110,471,003

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)
nssv158134784.6e-005121694
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