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nsv5410872

  • 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: 78 SVs from 18 studies. See in: genome view    
Submitted genomic41,828,827-41,828,878Question Mark
Overlapping variant regions from other studies: 78 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):41,796,565-41,796,616Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5410872Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr641,828,82741,828,878
nsv5410872RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr641,796,56541,796,616

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16983176alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16983176Submitted genomicNC_000006.12:g.418
28827_41828878ins2
78
GRCh38 (hg38)NC_000006.12Chr641,828,82741,828,878
nssv16983176RemappedPerfectNC_000006.11:g.417
96565_41796616ins2
78
GRCh37.p13First PassNC_000006.11Chr641,796,56541,796,616

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)
nssv169831760.005296404
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