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nsv5423904

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:657

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 105 SVs from 21 studies. See in: genome view    
Submitted genomic116,915,050-116,915,706Question Mark
Overlapping variant regions from other studies: 107 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):117,457,672-117,458,328Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5423904Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1116,915,050116,915,706
nsv5423904RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1117,457,672117,458,328

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16889640deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16889640Submitted genomicNC_000001.11:g.116
915050_116915706de
l
GRCh38 (hg38)NC_000001.11Chr1116,915,050116,915,706
nssv16889640RemappedPerfectNC_000001.10:g.117
457672_117458328de
l
GRCh37.p13First PassNC_000001.10Chr1117,457,672117,458,328

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)
nssv16889640<0.00116404
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