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nsv5544481

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:44

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 248 SVs from 31 studies. See in: genome view    
Submitted genomic31,312,227-31,312,270Question Mark
Overlapping variant regions from other studies: 248 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):29,639,245-29,639,288Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5544481Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1731,312,22731,312,270
nsv5544481RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1729,639,24529,639,288

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17712566insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17712566Submitted genomicNC_000017.11:g.313
12227_31312270ins3
20
GRCh38 (hg38)NC_000017.11Chr1731,312,22731,312,270
nssv17712566RemappedPerfectNC_000017.10:g.296
39245_29639288ins3
20
GRCh37.p13First PassNC_000017.10Chr1729,639,24529,639,288

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)
nssv17712566<0.00136404
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