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nsv4221205

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:101,391

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 89 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):119,565,298-119,666,688Question Mark
Overlapping variant regions from other studies: 89 SVs from 15 studies. See in: genome view    
Submitted genomic120,003,103-120,104,493Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4221205RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr12119,565,298119,666,688
nsv4221205Submitted genomicGRCh37.p13Primary AssemblyNC_000012.11Chr12120,003,103120,104,493

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15949500duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15949500RemappedPerfectNC_000012.12:g.119
565298_119666688du
p
GRCh38.p12First PassNC_000012.12Chr12119,565,298119,666,688
nssv15949500Submitted genomicNC_000012.11:g.120
003103_120104493du
p
GRCh37.p13NC_000012.11Chr12120,003,103120,104,493

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)
nssv159495004.6e-005121694
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