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nsv5533607

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,824

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 144 SVs from 28 studies. See in: genome view    
Submitted genomic76,268,596-76,274,419Question Mark
Overlapping variant regions from other studies: 144 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):74,264,677-74,270,500Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5533607Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1776,268,59676,274,419
nsv5533607RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1774,264,67774,270,500

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714702deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714702Submitted genomicNC_000017.11:g.762
68596_76274419del
GRCh38 (hg38)NC_000017.11Chr1776,268,59676,274,419
nssv17714702RemappedPerfectNC_000017.10:g.742
64677_74270500del
GRCh37.p13First PassNC_000017.10Chr1774,264,67774,270,500

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)
nssv17714702<0.00116404
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