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nsv5433985

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:190

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 113 SVs from 22 studies. See in: genome view    
Submitted genomic128,755,844-128,756,033Question Mark
Overlapping variant regions from other studies: 113 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):128,474,687-128,474,876Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5433985Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3128,755,844128,756,033
nsv5433985RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3128,474,687128,474,876

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16939834deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16939834Submitted genomicNC_000003.12:g.128
755844_128756033de
l
GRCh38 (hg38)NC_000003.12Chr3128,755,844128,756,033
nssv16939834RemappedPerfectNC_000003.11:g.128
474687_128474876de
l
GRCh37.p13First PassNC_000003.11Chr3128,474,687128,474,876

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)
nssv16939834<0.00116404
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