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nsv5412721

  • 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: 118 SVs from 21 studies. See in: genome view    
Submitted genomic19,143,133-19,143,184Question Mark
Overlapping variant regions from other studies: 118 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):19,143,364-19,143,415Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5412721Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr619,143,13319,143,184
nsv5412721RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr619,143,36419,143,415

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16980704alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16980704Submitted genomicNC_000006.12:g.191
43133_19143184ins2
81
GRCh38 (hg38)NC_000006.12Chr619,143,13319,143,184
nssv16980704RemappedPerfectNC_000006.11:g.191
43364_19143415ins2
81
GRCh37.p13First PassNC_000006.11Chr619,143,36419,143,415

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)
nssv16980704<0.00116404
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