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nsv5404062

  • 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 24 studies. See in: genome view    
Submitted genomic16,656,643-16,656,694Question Mark
Overlapping variant regions from other studies: 136 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):16,696,268-16,696,319Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5404062Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr716,656,64316,656,694
nsv5404062RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr716,696,26816,696,319

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16993837alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16993837Submitted genomicNC_000007.14:g.166
56643_16656694ins2
79
GRCh38 (hg38)NC_000007.14Chr716,656,64316,656,694
nssv16993837RemappedPerfectNC_000007.13:g.166
96268_16696319ins2
79
GRCh37.p13First PassNC_000007.13Chr716,696,26816,696,319

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)
nssv16993837<0.00116404
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