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nsv4878267

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:72,519,398

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 189732 SVs from 154 studies. See in: genome view    
Remapped(Score: Good):45,103,677-117,623,076Question Mark
Overlapping variant regions from other studies: 189642 SVs from 154 studies. See in: genome view    
Submitted genomic45,105,694-118,544,231Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4878267RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr445,103,678 (-1)117,623,075 (+1)
nsv4878267Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000004.11Chr445,105,695 (-1)118,544,230 (+1)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16411839inversionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16411839RemappedGoodNC_000004.12:g.(45
103677_?)_(?_11762
3076)inv
GRCh38.p12First PassNC_000004.12Chr445,103,678 (-1)117,623,075 (+1)
nssv16411839Submitted genomicNC_000004.11:g.(45
105694_?)_(?_11854
4231)inv
GRCh37 (hg19)NC_000004.11Chr445,105,695 (-1)118,544,230 (+1)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16411839<0.001116834
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