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nsv5418465

  • 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: 107 SVs from 30 studies. See in: genome view    
Submitted genomic52,827,314-52,827,365Question Mark
Overlapping variant regions from other studies: 107 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):53,221,098-53,221,149Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5418465Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1252,827,31452,827,365
nsv5418465RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1253,221,09853,221,149

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058291alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058291Submitted genomicNC_000012.12:g.528
27314_52827365ins2
80
GRCh38 (hg38)NC_000012.12Chr1252,827,31452,827,365
nssv17058291RemappedPerfectNC_000012.11:g.532
21098_53221149ins2
80
GRCh37.p13First PassNC_000012.11Chr1253,221,09853,221,149

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)
nssv170582910.008546404
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