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nsv5398472

  • 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: 190 SVs from 39 studies. See in: genome view    
Submitted genomic92,005,018-92,005,069Question Mark
Overlapping variant regions from other studies: 190 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):92,470,575-92,470,626Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5398472Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr192,005,01892,005,069
nsv5398472RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr192,470,57592,470,626

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16906444alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16906444Submitted genomicNC_000001.11:g.920
05018_92005069ins2
81
GRCh38 (hg38)NC_000001.11Chr192,005,01892,005,069
nssv16906444RemappedPerfectNC_000001.10:g.924
70575_92470626ins2
81
GRCh37.p13First PassNC_000001.10Chr192,470,57592,470,626

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)
nssv16906444<0.00136404
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