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nsv5446857

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:316

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 155 SVs from 24 studies. See in: genome view    
Submitted genomic224,150,167-224,150,482Question Mark
Overlapping variant regions from other studies: 158 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):224,337,869-224,338,184Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5446857Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1224,150,167224,150,482
nsv5446857RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1224,337,869224,338,184

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16896373deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16896373Submitted genomicNC_000001.11:g.224
150167_224150482de
l
GRCh38 (hg38)NC_000001.11Chr1224,150,167224,150,482
nssv16896373RemappedPerfectNC_000001.10:g.224
337869_224338184de
l
GRCh37.p13First PassNC_000001.10Chr1224,337,869224,338,184

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)
nssv16896373<0.00146404
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