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nsv5483102

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:124

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 181 SVs from 23 studies. See in: genome view    
Submitted genomic102,209,352-102,209,475Question Mark
Overlapping variant regions from other studies: 181 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):103,221,580-103,221,703Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5483102Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8102,209,352102,209,475
nsv5483102RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8103,221,580103,221,703

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17015761deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17015761Submitted genomicNC_000008.11:g.102
209352_102209475de
l
GRCh38 (hg38)NC_000008.11Chr8102,209,352102,209,475
nssv17015761RemappedPerfectNC_000008.10:g.103
221580_103221703de
l
GRCh37.p13First PassNC_000008.10Chr8103,221,580103,221,703

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)
nssv17015761<0.00156404
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