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nsv5530868

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:56

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 103 SVs from 22 studies. See in: genome view    
Submitted genomic30,462,141-30,462,196Question Mark
Overlapping variant regions from other studies: 103 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):28,789,159-28,789,214Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5530868Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1730,462,14130,462,196
nsv5530868RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1728,789,15928,789,214

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17712481deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17712481Submitted genomicNC_000017.11:g.304
62141_30462196del
GRCh38 (hg38)NC_000017.11Chr1730,462,14130,462,196
nssv17712481RemappedPerfectNC_000017.10:g.287
89159_28789214del
GRCh37.p13First PassNC_000017.10Chr1728,789,15928,789,214

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)
nssv17712481<0.00116404
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