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nsv5427440

  • 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: 101 SVs from 27 studies. See in: genome view    
Submitted genomic52,804,884-52,804,935Question Mark
Overlapping variant regions from other studies: 101 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):53,198,668-53,198,719Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5427440Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1252,804,88452,804,935
nsv5427440RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1253,198,66853,198,719

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058802alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058802Submitted genomicNC_000012.12:g.528
04884_52804935ins1
96
GRCh38 (hg38)NC_000012.12Chr1252,804,88452,804,935
nssv17058802RemappedPerfectNC_000012.11:g.531
98668_53198719ins1
96
GRCh37.p13First PassNC_000012.11Chr1253,198,66853,198,719

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)
nssv170588020.00186404
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