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nsv4230843

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:117,432

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 223 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):98,538,520-98,655,951Question Mark
Overlapping variant regions from other studies: 223 SVs from 20 studies. See in: genome view    
Submitted genomic98,932,298-99,049,729Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4230843RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1298,538,52098,655,951
nsv4230843Submitted genomicGRCh37.p13Primary AssemblyNC_000012.11Chr1298,932,29899,049,729

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15955207duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15955207RemappedPerfectNC_000012.12:g.985
38520_98655951dup
GRCh38.p12First PassNC_000012.12Chr1298,538,52098,655,951
nssv15955207Submitted genomicNC_000012.11:g.989
32298_99049729dup
GRCh37.p13NC_000012.11Chr1298,932,29899,049,729

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)
nssv159552074.6e-005121694
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