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nsv5438209

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:189

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 145 SVs from 25 studies. See in: genome view    
Submitted genomic227,767,445-227,767,633Question Mark
Overlapping variant regions from other studies: 148 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):227,955,146-227,955,334Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5438209Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1227,767,445227,767,633
nsv5438209RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1227,955,146227,955,334

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16897464deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16897464Submitted genomicNC_000001.11:g.227
767445_227767633de
l
GRCh38 (hg38)NC_000001.11Chr1227,767,445227,767,633
nssv16897464RemappedPerfectNC_000001.10:g.227
955146_227955334de
l
GRCh37.p13First PassNC_000001.10Chr1227,955,146227,955,334

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)
nssv16897464<0.00146404
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