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nsv5526907

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,601

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 181 SVs from 23 studies. See in: genome view    
Submitted genomic45,974,919-45,982,519Question Mark
Overlapping variant regions from other studies: 181 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):43,554,885-43,562,485Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5526907Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1845,974,91945,982,519
nsv5526907RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1843,554,88543,562,485

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17717870duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17717870Submitted genomicNC_000018.10:g.459
74919_45982519dup
GRCh38 (hg38)NC_000018.10Chr1845,974,91945,982,519
nssv17717870RemappedPerfectNC_000018.9:g.4355
4885_43562485dup
GRCh37.p13First PassNC_000018.9Chr1843,554,88543,562,485

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)
nssv17717870<0.00126404
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