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nsv5553476

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:339

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 204 SVs from 21 studies. See in: genome view    
Submitted genomic45,955,146-45,955,484Question Mark
Overlapping variant regions from other studies: 204 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):46,351,026-46,351,364Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5553476Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2245,955,14645,955,484
nsv5553476RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2246,351,02646,351,364

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17729523deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17729523Submitted genomicNC_000022.11:g.459
55146_45955484del
GRCh38 (hg38)NC_000022.11Chr2245,955,14645,955,484
nssv17729523RemappedPerfectNC_000022.10:g.463
51026_46351364del
GRCh37.p13First PassNC_000022.10Chr2246,351,02646,351,364

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)
nssv17729523<0.00116404
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