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nsv5547030

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:44,898,008

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 114110 SVs from 145 studies. See in: genome view    
Submitted genomic68,996,170-113,894,177Question Mark
Overlapping variant regions from other studies: 114118 SVs from 145 studies. See in: genome view    
Remapped(Score: Good):69,861,888-114,815,333Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5547030Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr468,996,170113,894,177
nsv5547030RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr469,861,888114,815,333

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16950558insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16950558Submitted genomicNC_000004.12:g.689
96170_113894177ins
70
GRCh38 (hg38)NC_000004.12Chr468,996,170113,894,177
nssv16950558RemappedGoodNC_000004.11:g.698
61888_114815333ins
70
GRCh37.p13First PassNC_000004.11Chr469,861,888114,815,333

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)
nssv169505580.23810474404
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