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nsv5399185

  • 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: 136 SVs from 29 studies. See in: genome view    
Submitted genomic66,958,452-66,958,503Question Mark
Overlapping variant regions from other studies: 136 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):67,424,135-67,424,186Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5399185Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr166,958,45266,958,503
nsv5399185RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr167,424,13567,424,186

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16903980alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16903980Submitted genomicNC_000001.11:g.669
58452_66958503ins2
81
GRCh38 (hg38)NC_000001.11Chr166,958,45266,958,503
nssv16903980RemappedPerfectNC_000001.10:g.674
24135_67424186ins2
81
GRCh37.p13First PassNC_000001.10Chr167,424,13567,424,186

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)
nssv16903980<0.00156398
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