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nsv5486571

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:97

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 85 SVs from 22 studies. See in: genome view    
Submitted genomic91,168,647-91,168,743Question Mark
Overlapping variant regions from other studies: 85 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):92,928,404-92,928,500Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5486571Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1091,168,64791,168,743
nsv5486571RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1092,928,40492,928,500

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17036873deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17036873Submitted genomicNC_000010.11:g.911
68647_91168743del
GRCh38 (hg38)NC_000010.11Chr1091,168,64791,168,743
nssv17036873RemappedPerfectNC_000010.10:g.929
28404_92928500del
GRCh37.p13First PassNC_000010.10Chr1092,928,40492,928,500

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)
nssv17036873<0.00116404
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