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nsv5515620

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:300

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 146 SVs from 38 studies. See in: genome view    
Submitted genomic77,992,217-77,992,516Question Mark
Overlapping variant regions from other studies: 146 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):75,988,298-75,988,597Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5515620Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1777,992,21777,992,516
nsv5515620RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1775,988,29875,988,597

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714819deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714819Submitted genomicNC_000017.11:g.779
92217_77992516del
GRCh38 (hg38)NC_000017.11Chr1777,992,21777,992,516
nssv17714819RemappedPerfectNC_000017.10:g.759
88298_75988597del
GRCh37.p13First PassNC_000017.10Chr1775,988,29875,988,597

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)
nssv177148190.48731186404
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