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nsv5417340

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:117

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 116 SVs from 17 studies. See in: genome view    
Submitted genomic100,363,312-100,363,428Question Mark
Overlapping variant regions from other studies: 116 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):100,828,868-100,828,984Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5417340Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1100,363,312100,363,428
nsv5417340RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1100,828,868100,828,984

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16907050deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16907050Submitted genomicNC_000001.11:g.100
363312_100363428de
l
GRCh38 (hg38)NC_000001.11Chr1100,363,312100,363,428
nssv16907050RemappedPerfectNC_000001.10:g.100
828868_100828984de
l
GRCh37.p13First PassNC_000001.10Chr1100,828,868100,828,984

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)
nssv16907050<0.00146404
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