nsv5410436

  • 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: 86 SVs from 27 studies. See in: genome view    
Submitted genomic79,465,518-79,465,569Question Mark
Overlapping variant regions from other studies: 86 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):79,094,834-79,094,885Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5410436Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr779,465,51879,465,569
nsv5410436RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr779,094,83479,094,885

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16998851alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16998851Submitted genomicNC_000007.14:g.794
65518_79465569ins2
81
GRCh38 (hg38)NC_000007.14Chr779,465,51879,465,569
nssv16998851RemappedPerfectNC_000007.13:g.790
94834_79094885ins2
81
GRCh37.p13First PassNC_000007.13Chr779,094,83479,094,885

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)
nssv16998851<0.00126404
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