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nsv5446328

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,023

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 119 SVs from 23 studies. See in: genome view    
Submitted genomic207,041,227-207,043,249Question Mark
Overlapping variant regions from other studies: 123 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):207,214,572-207,216,594Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5446328Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1207,041,227207,043,249
nsv5446328RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1207,214,572207,216,594

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16894964deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16894964Submitted genomicNC_000001.11:g.207
041227_207043249de
l
GRCh38 (hg38)NC_000001.11Chr1207,041,227207,043,249
nssv16894964RemappedPerfectNC_000001.10:g.207
214572_207216594de
l
GRCh37.p13First PassNC_000001.10Chr1207,214,572207,216,594

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)
nssv16894964<0.00116404
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