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nsv5558888

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 114 SVs from 18 studies. See in: genome view    
Submitted genomic28,741,645-28,741,696Question Mark
Overlapping variant regions from other studies: 114 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):28,964,511-28,964,562Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5558888Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr228,741,64528,741,696
nsv5558888RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr228,964,51128,964,562

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16911356line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16911356Submitted genomicNC_000002.12:g.287
41645_28741696ins6
019
GRCh38 (hg38)NC_000002.12Chr228,741,64528,741,696
nssv16911356RemappedPerfectNC_000002.11:g.289
64511_28964562ins6
019
GRCh37.p13First PassNC_000002.11Chr228,964,51128,964,562

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)
nssv16911356<0.00136404
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