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nsv6147285

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,983

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 252 SVs from 34 studies. See in: genome view    
Submitted genomic5,485,852-5,495,834Question Mark
Overlapping variant regions from other studies: 252 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):5,487,579-5,497,561Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6147285Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr45,485,8525,495,834
nsv6147285RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr45,487,5795,497,561

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16945763mobile element deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16945763Submitted genomicNC_000004.12:g.548
5852_5495834del
GRCh38 (hg38)NC_000004.12Chr45,485,8525,495,834
nssv16945763RemappedPerfectNC_000004.11:g.548
7579_5497561del
GRCh37.p13First PassNC_000004.11Chr45,487,5795,497,561

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)
nssv16945763<0.00146404
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