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nsv5405512

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 435 SVs from 34 studies. See in: genome view    
Submitted genomic1,786,424-1,786,475Question Mark
Overlapping variant regions from other studies: 435 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):1,717,863-1,717,914Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5405512Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr11,786,4241,786,475
nsv5405512RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr11,717,8631,717,914

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16902517alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16902517Submitted genomicNC_000001.11:g.178
6424_1786475ins280
GRCh38 (hg38)NC_000001.11Chr11,786,4241,786,475
nssv16902517RemappedPerfectNC_000001.10:g.171
7863_1717914ins280
GRCh37.p13First PassNC_000001.10Chr11,717,8631,717,914

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)
nssv16902517<0.00116404
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