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nsv5423217

  • 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: 724 SVs from 52 studies. See in: genome view    
Submitted genomic15,872,800-15,872,851Question Mark
Overlapping variant regions from other studies: 724 SVs from 52 studies. See in: genome view    
Remapped(Score: Perfect):15,966,657-15,966,708Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5423217Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1615,872,80015,872,851
nsv5423217RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1615,966,65715,966,708

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17705024alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17705024Submitted genomicNC_000016.10:g.158
72800_15872851ins2
80
GRCh38 (hg38)NC_000016.10Chr1615,872,80015,872,851
nssv17705024RemappedPerfectNC_000016.9:g.1596
6657_15966708ins28
0
GRCh37.p13First PassNC_000016.9Chr1615,966,65715,966,708

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)
nssv17705024<0.00116404
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