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nsv5452153

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:206

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 120 SVs from 20 studies. See in: genome view    
Submitted genomic221,424,954-221,425,159Question Mark
Overlapping variant regions from other studies: 120 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):222,289,674-222,289,879Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5452153Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2221,424,954221,425,159
nsv5452153RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2222,289,674222,289,879

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16928312deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16928312Submitted genomicNC_000002.12:g.221
424954_221425159de
l
GRCh38 (hg38)NC_000002.12Chr2221,424,954221,425,159
nssv16928312RemappedPerfectNC_000002.11:g.222
289674_222289879de
l
GRCh37.p13First PassNC_000002.11Chr2222,289,674222,289,879

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)
nssv169283120.01656404
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