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nsv5441161

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,710

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 157 SVs from 33 studies. See in: genome view    
Submitted genomic112,915,307-112,920,016Question Mark
Overlapping variant regions from other studies: 157 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):112,634,154-112,638,863Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5441161Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3112,915,307112,920,016
nsv5441161RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3112,634,154112,638,863

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16938338deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16938338Submitted genomicNC_000003.12:g.112
915307_112920016de
l
GRCh38 (hg38)NC_000003.12Chr3112,915,307112,920,016
nssv16938338RemappedPerfectNC_000003.11:g.112
634154_112638863de
l
GRCh37.p13First PassNC_000003.11Chr3112,634,154112,638,863

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)
nssv16938338<0.00136404
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