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nsv5401184

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:37

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 147 SVs from 20 studies. See in: genome view    
Submitted genomic178,478,163-178,478,199Question Mark
Overlapping variant regions from other studies: 149 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):178,447,298-178,447,334Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5401184Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1178,478,163178,478,199
nsv5401184RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1178,447,298178,447,334

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16892984alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16892984Submitted genomicNC_000001.11:g.178
478163_178478199in
s303
GRCh38 (hg38)NC_000001.11Chr1178,478,163178,478,199
nssv16892984RemappedPerfectNC_000001.10:g.178
447298_178447334in
s303
GRCh37.p13First PassNC_000001.10Chr1178,447,298178,447,334

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)
nssv168929840.003226404
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