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nsv5427642

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:920

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 800 SVs from 65 studies. See in: genome view    
Submitted genomic1,725,159-1,726,078Question Mark
Overlapping variant regions from other studies: 800 SVs from 65 studies. See in: genome view    
Remapped(Score: Perfect):1,656,598-1,657,517Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5427642Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr11,725,1591,726,078
nsv5427642RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr11,656,5981,657,517

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16902511deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16902511Submitted genomicNC_000001.11:g.172
5159_1726078del
GRCh38 (hg38)NC_000001.11Chr11,725,1591,726,078
nssv16902511RemappedPerfectNC_000001.10:g.165
6598_1657517del
GRCh37.p13First PassNC_000001.10Chr11,656,5981,657,517

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)
nssv169025110.008496404
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