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nsv5407333

  • 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: 236 SVs from 26 studies. See in: genome view    
Submitted genomic17,905,443-17,905,494Question Mark
Overlapping variant regions from other studies: 236 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):17,762,952-17,763,003Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5407333Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr817,905,44317,905,494
nsv5407333RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr817,762,95217,763,003

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17007554alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17007554Submitted genomicNC_000008.11:g.179
05443_17905494ins2
81
GRCh38 (hg38)NC_000008.11Chr817,905,44317,905,494
nssv17007554RemappedPerfectNC_000008.10:g.177
62952_17763003ins2
81
GRCh37.p13First PassNC_000008.10Chr817,762,95217,763,003

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)
nssv17007554<0.00116404
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