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nsv5445972

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,761

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 138 SVs from 23 studies. See in: genome view    
Submitted genomic201,048,489-201,050,249Question Mark
Overlapping variant regions from other studies: 138 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):201,913,212-201,914,972Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5445972Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2201,048,489201,050,249
nsv5445972RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2201,913,212201,914,972

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16922876deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16922876Submitted genomicNC_000002.12:g.201
048489_201050249de
l
GRCh38 (hg38)NC_000002.12Chr2201,048,489201,050,249
nssv16922876RemappedPerfectNC_000002.11:g.201
913212_201914972de
l
GRCh37.p13First PassNC_000002.11Chr2201,913,212201,914,972

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)
nssv16922876<0.00116404
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