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nsv5403253

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 122 SVs from 21 studies. See in: genome view    
Submitted genomic44,332,262-44,332,313Question Mark
Overlapping variant regions from other studies: 122 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):44,797,934-44,797,985Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5403253Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr144,332,26244,332,313
nsv5403253RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr144,797,93444,797,985

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16902561alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16902561Submitted genomicNC_000001.11:g.443
32262_44332313ins2
80
GRCh38 (hg38)NC_000001.11Chr144,332,26244,332,313
nssv16902561RemappedPerfectNC_000001.10:g.447
97934_44797985ins2
80
GRCh37.p13First PassNC_000001.10Chr144,797,93444,797,985

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)
nssv16902561<0.00116404
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