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nsv5547709

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:167

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 135 SVs from 25 studies. See in: genome view    
Submitted genomic73,114,670-73,114,836Question Mark
Overlapping variant regions from other studies: 135 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):73,148,569-73,148,735Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5547709Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1673,114,67073,114,836
nsv5547709RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1673,148,56973,148,735

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17707243insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17707243Submitted genomicNC_000016.10:g.731
14670_73114836ins2
47
GRCh38 (hg38)NC_000016.10Chr1673,114,67073,114,836
nssv17707243RemappedPerfectNC_000016.9:g.7314
8569_73148735ins24
7
GRCh37.p13First PassNC_000016.9Chr1673,148,56973,148,735

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)
nssv17707243<0.00116404
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