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nsv5451826

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:24,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 162 SVs from 30 studies. See in: genome view    
Submitted genomic232,153,618-232,177,618Question Mark
Overlapping variant regions from other studies: 162 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):233,018,328-233,042,328Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5451826Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2232,153,618232,177,618
nsv5451826RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2233,018,328233,042,328

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16928595deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16928595Submitted genomicNC_000002.12:g.232
153618_232177618de
l
GRCh38 (hg38)NC_000002.12Chr2232,153,618232,177,618
nssv16928595RemappedPerfectNC_000002.11:g.233
018328_233042328de
l
GRCh37.p13First PassNC_000002.11Chr2233,018,328233,042,328

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)
nssv16928595<0.00116404
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