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nsv5486241

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:275

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 83 SVs from 22 studies. See in: genome view    
Submitted genomic96,521,588-96,521,862Question Mark
Overlapping variant regions from other studies: 83 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):98,281,345-98,281,619Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5486241Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1096,521,58896,521,862
nsv5486241RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1098,281,34598,281,619

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17039741deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17039741Submitted genomicNC_000010.11:g.965
21588_96521862del
GRCh38 (hg38)NC_000010.11Chr1096,521,58896,521,862
nssv17039741RemappedPerfectNC_000010.10:g.982
81345_98281619del
GRCh37.p13First PassNC_000010.10Chr1098,281,34598,281,619

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)
nssv17039741<0.00166404
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