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nsv5556753

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 88 SVs from 18 studies. See in: genome view    
Submitted genomic11,746,551-11,746,566Question Mark
Overlapping variant regions from other studies: 88 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):11,857,366-11,857,381Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5556753Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1911,746,55111,746,566
nsv5556753RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1911,857,36611,857,381

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17721441mobile element insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17721441Submitted genomicNC_000019.10:g.117
46551_11746566ins5
8
GRCh38 (hg38)NC_000019.10Chr1911,746,55111,746,566
nssv17721441RemappedPerfectNC_000019.9:g.1185
7366_11857381ins58
GRCh37.p13First PassNC_000019.9Chr1911,857,36611,857,381

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)
nssv177214410.0855065950
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