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nsv5443560

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,398

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 99 SVs from 17 studies. See in: genome view    
Submitted genomic119,469,910-119,471,307Question Mark
Overlapping variant regions from other studies: 99 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):119,188,757-119,190,154Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5443560Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3119,469,910119,471,307
nsv5443560RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3119,188,757119,190,154

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16939450deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16939450Submitted genomicNC_000003.12:g.119
469910_119471307de
l
GRCh38 (hg38)NC_000003.12Chr3119,469,910119,471,307
nssv16939450RemappedPerfectNC_000003.11:g.119
188757_119190154de
l
GRCh37.p13First PassNC_000003.11Chr3119,188,757119,190,154

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)
nssv16939450<0.00116404
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